Abnormal accumulation of serous fluid in two or more fetal compartments, such as SKIN; PLEURA; PERICARDIUM; PLACENTA; PERITONEUM; AMNIOTIC FLUID. General fetal EDEMA may be of non-immunologic origin, or of immunologic origin as in the case of ERYTHROBLASTOSIS FETALIS.
An accumulation of ENDOLYMPH in the inner ear (LABYRINTH) leading to buildup of pressure and distortion of intralabyrinthine structures, such as COCHLEA and SEMICIRCULAR CANALS. It is characterized by SENSORINEURAL HEARING LOSS; TINNITUS; and sometimes VERTIGO.
Pathophysiological conditions of the FETUS in the UTERUS. Some fetal diseases may be treated with FETAL THERAPIES.
The type species of ERYTHROVIRUS and the etiological agent of ERYTHEMA INFECTIOSUM, a disease most commonly seen in school-age children.
Virus infections caused by the PARVOVIRIDAE.
In utero transfusion of BLOOD into the FETUS for the treatment of FETAL DISEASES, such as fetal erythroblastosis (ERYTHROBLASTOSIS, FETAL).
A condition characterized by the abnormal presence of ERYTHROBLASTS in the circulation of the FETUS or NEWBORNS. It is a disorder due to BLOOD GROUP INCOMPATIBILITY, such as the maternal alloimmunization by fetal antigen RH FACTORS leading to HEMOLYSIS of ERYTHROCYTES, hemolytic anemia (ANEMIA, HEMOLYTIC), general edema (HYDROPS FETALIS), and SEVERE JAUNDICE IN NEWBORN.
A disorder characterized by reduced synthesis of the alpha chains of hemoglobin. The severity of this condition can vary from mild anemia to death, depending on the number of genes deleted.
The process by which fetal Rh+ erythrocytes enter the circulation of an Rh- mother, causing her to produce IMMUNOGLOBULIN G antibodies, which can cross the placenta and destroy the erythrocytes of Rh+ fetuses. Rh isoimmunization can also be caused by BLOOD TRANSFUSION with mismatched blood.
Hemoglobins characterized by structural alterations within the molecule. The alteration can be either absence, addition or substitution of one or more amino acids in the globin part of the molecule at selected positions in the polypeptide chains.
Contagious infection with human B19 Parvovirus most commonly seen in school age children and characterized by fever, headache, and rashes of the face, trunk, and extremities. It is often confused with rubella.
Death of the developing young in utero. BIRTH of a dead FETUS is STILLBIRTH.
A collection of watery fluid in the pleural cavity. (Dorland, 27th ed)
An abnormality in lung development that is characterized by a multicystic mass resulting from an adenomatous overgrowth of the terminal BRONCHIOLES with a consequent reduction of PULMONARY ALVEOLI. This anomaly is classified into three types by the cyst size.
Determination of the nature of a pathological condition or disease in the postimplantation EMBRYO; FETUS; or pregnant female before birth.
A condition of abnormally high AMNIOTIC FLUID volume, such as greater than 2,000 ml in the LAST TRIMESTER and usually diagnosed by ultrasonographic criteria (AMNIOTIC FLUID INDEX). It is associated with maternal DIABETES MELLITUS; MULTIPLE PREGNANCY; CHROMOSOMAL DISORDERS; and congenital abnormalities.
The visualization of tissues during pregnancy through recording of the echoes of ultrasonic waves directed into the body. The procedure may be applied with reference to the mother or the fetus and with reference to organs or the detection of maternal or fetal disease.
The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH.
Members of the alpha-globin family. In humans, they are encoded in a gene cluster on CHROMOSOME 16. They include zeta-globin and alpha-globin. There are also pseudogenes of zeta (theta-zeta) and alpha (theta-alpha) in the cluster. Adult HEMOGLOBIN is comprised of 2 alpha-globin chains and 2 beta-globin chains.
An abnormal hemoglobin composed of four beta chains. It is caused by the reduced synthesis of the alpha chain. This abnormality results in ALPHA-THALASSEMIA.
Abnormal fluid accumulation in TISSUES or body cavities. Most cases of edema are present under the SKIN in SUBCUTANEOUS TISSUE.
Abortion performed because of possible fetal defects.
Mucopolysaccharidosis characterized by excessive dermatan and heparan sulfates in the urine and Hurler-like features. It is caused by a deficiency of beta-glucuronidase.
An infant during the first month after birth.
A group of enzymes that catalyze an intramolecular transfer of a phosphate group. It has been shown in some cases that the enzyme has a functional phosphate group, which can act as the donor. These were previously listed under PHOSPHOTRANSFERASES (EC 2.7.-). (From Enzyme Nomenclature, 1992) EC 5.4.2.
A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains. There are several genetic types with clinical pictures ranging from barely detectable hematologic abnormality to severe and fatal anemia.
A condition in which albumin level in blood (SERUM ALBUMIN) is below the normal range. Hypoalbuminemia may be due to decreased hepatic albumin synthesis, increased albumin catabolism, altered albumin distribution, or albumin loss through the urine (ALBUMINURIA).
The age of the conceptus, beginning from the time of FERTILIZATION. In clinical obstetrics, the gestational age is often estimated as the time from the last day of the last MENSTRUATION which is about 2 weeks before OVULATION and fertilization.
Percutaneous transabdominal puncture of the uterus during pregnancy to obtain amniotic fluid. It is commonly used for fetal karyotype determination in order to diagnose abnormal fetal conditions.
A disease of the inner ear (LABYRINTH) that is characterized by fluctuating SENSORINEURAL HEARING LOSS; TINNITUS; episodic VERTIGO; and aural fullness. It is the most common form of endolymphatic hydrops.
Death resulting from the presence of a disease in an individual, as shown by a single case report or a limited number of patients. This should be differentiated from DEATH, the physiological cessation of life and from MORTALITY, an epidemiological or statistical concept.
The co-occurrence of pregnancy and an INFECTION. The infection may precede or follow FERTILIZATION.
Congenital or acquired structural abnormalities of the lymphatic system (LYMPHOID TISSUE) including the lymph vessels.
Developmental abnormalities in any portion of the ATRIAL SEPTUM resulting in abnormal communications between the two upper chambers of the heart. Classification of atrial septal defects is based on location of the communication and types of incomplete fusion of atrial septa with the ENDOCARDIAL CUSHIONS in the fetal heart. They include ostium primum, ostium secundum, sinus venosus, and coronary sinus defects.
Developmental abnormalities in any portion of the VENTRICULAR SEPTUM resulting in abnormal communications between the two lower chambers of the heart. Classification of ventricular septal defects is based on location of the communication, such as perimembranous, inlet, outlet (infundibular), central muscular, marginal muscular, or apical muscular defect.
A condition of markedly elevated BLOOD PRESSURE with DIASTOLIC PRESSURE usually greater than 120 mm Hg. Malignant hypertension is characterized by widespread vascular damage, PAPILLEDEMA, retinopathy, HYPERTENSIVE ENCEPHALOPATHY, and renal dysfunction.
A group of diseases in which the dominant feature is the involvement of the CARDIAC MUSCLE itself. Cardiomyopathies are classified according to their predominant pathophysiological features (DILATED CARDIOMYOPATHY; HYPERTROPHIC CARDIOMYOPATHY; RESTRICTIVE CARDIOMYOPATHY) or their etiological/pathological factors (CARDIOMYOPATHY, ALCOHOLIC; ENDOCARDIAL FIBROELASTOSIS).
A characteristic symptom complex.
A human infant born before 37 weeks of GESTATION.
A condition in which the HEAD of the FETUS is larger than the mother's PELVIS through which the fetal head must pass during a vaginal delivery.
Measurement of the dimensions and capacity of the pelvis. It includes cephalopelvimetry (measurement of fetal head size in relation to maternal pelvic capacity), a prognostic guide to the management of LABOR, OBSTETRIC associated with disproportion.
Removal of the fetus from the uterus or vagina at or near the end of pregnancy with a metal traction cup that is attached to the fetus' head. Negative pressure is applied and traction is made on a chain passed through the suction tube. (From Stedman, 26th ed & Dorland, 28th ed)
A spectrum of congenital, inherited, or acquired abnormalities in BLOOD VESSELS that can adversely affect the normal blood flow in ARTERIES or VEINS. Most are congenital defects such as abnormal communications between blood vessels (fistula), shunting of arterial blood directly into veins bypassing the CAPILLARIES (arteriovenous malformations), formation of large dilated blood blood-filled vessels (cavernous angioma), and swollen capillaries (capillary telangiectases). In rare cases, vascular malformations can result from trauma or diseases.
Erythrocyte isoantigens of the Rh (Rhesus) blood group system, the most complex of all human blood groups. The major antigen Rh or D is the most common cause of erythroblastosis fetalis.
Female parents, human or animal.
The major human blood type system which depends on the presence or absence of two antigens A and B. Type O occurs when neither A nor B is present and AB when both are present. A and B are genetic factors that determine the presence of enzymes for the synthesis of certain glycoproteins mainly in the red cell membrane.
Sets of cell surface antigens located on BLOOD CELLS. They are usually membrane GLYCOPROTEINS or GLYCOLIPIDS that are antigenically distinguished by their carbohydrate moieties.
The unborn young of a viviparous mammal, in the postembryonic period, after the major structures have been outlined. In humans, the unborn young from the end of the eighth week after CONCEPTION until BIRTH, as distinguished from the earlier EMBRYO, MAMMALIAN.
A developmental abnormality in which the spiral (aortopulmonary) septum failed to completely divide the TRUNCUS ARTERIOSUS into ASCENDING AORTA and PULMONARY ARTERY. This abnormal communication between the two major vessels usually lies above their respective valves (AORTIC VALVE; PULMONARY VALVE).
A malformation of the heart in which the embryonic common PULMONARY VEIN was not incorporated into the LEFT ATRIUM leaving behind a perforated fibromuscular membrane bisecting the left atrium, a three-atrium heart. The opening between the two left atrium sections determines the degree of obstruction to pulmonary venous return, pulmonary venous and pulmonary arterial hypertension.
Presence of fluid in the pleural cavity resulting from excessive transudation or exudation from the pleural surfaces. It is a sign of disease and not a diagnosis in itself.

Fetal tachycardias: management and outcome of 127 consecutive cases. (1/193)

OBJECTIVE: To review the management and outcome of fetal tachycardia, and to determine the problems encountered with various treatment protocols. STUDY DESIGN: Retrospective analysis. SUBJECTS: 127 consecutive fetuses with a tachycardia presenting between 1980 and 1996 to a single tertiary centre for fetal cardiology. The median gestational age at presentation was 32 weeks (range 18 to 42). RESULTS: 105 fetuses had a supraventricular tachycardia and 22 had atrial flutter. Overall, 52 fetuses were hydropic and 75 non-hydropic. Prenatal control of the tachycardia was achieved in 83% of treated non-hydropic fetuses compared with 66% of the treated hydropic fetuses. Digoxin monotherapy converted most (62%) of the treated non-hydropic fetuses, and 96% survived through the neonatal period. First line drug treatment for hydropic fetuses was more diverse, including digoxin (n = 5), digoxin plus verapamil (n = 14), and flecainide (n = 27). The response rates to these drugs were 20%, 57%, and 59%, respectively, confirming that digoxin monotherapy is a poor choice for the hydropic fetus. Response to flecainide was faster than to the other drugs. Direct fetal treatment was used in four fetuses, of whom two survived. Overall, 73% (n = 38) of the hydropic fetuses survived. Postnatally, 4% of the non-hydropic group had ECG evidence of pre-excitation, compared with 16% of the hydropic group; 57% of non-hydropic fetuses were treated with long term anti-arrhythmics compared with 79% of hydropic fetuses. CONCLUSIONS: Non-hydropic fetuses with tachycardias have a very good prognosis with transplacental treatment. Most arrhythmias associated with fetal hydrops can be controlled with transplacental treatment, but the mortality in this group is 27%. At present, there is no ideal treatment protocol for these fetuses and a large prospective multicentre trial is required to optimise treatment of both hydropic and non-hydropic fetuses.  (+info)

Intrauterine management of fetal parvovirus B19 infection. (2/193)

OBJECTIVES: The aim of our study was to determine the outcome of pregnancies after intrauterine management of fetal parvovirus B19 infection. DESIGN: Retrospective study. SUBJECTS: A total of 37 cases of maternofetal parvovirus B19 infection, 35 of which were associated with hydrops fetalis, were referred to our tertiary level center between 1989 and 1996. With regard to fetal hydrops, no apparent cause other than parvovirus B19 infection was found in any patient. METHODS: In all patients, cordocentesis was performed to assess the degree of fetal anemia. When anemia was present, cordocentesis was followed by intrauterine transfusion with packed red cells into the umbilical vein. Further management depended on the degree of fetal anemia and gestational age and included follow-up fetal blood sampling/transfusion as well as ultrasound examinations as deemed appropriate. RESULTS: Packed red cell transfusion was performed in 30 patients with significant fetal anemia (Z-score 1.6-7.8 below the mean for gestational age). The fetal hemoglobin values ranged from 2.1 to 9.6 g/dl. Serum levels of platelets in the transfusion group were 9-228 x 10(9)/l with Z-scores in the range of < 1 to 3.8 below the mean. During treatment and follow-up, there were five intrauterine deaths (13.5%), one neonatal death (2.7%) and 31 live births (83.8%). CONCLUSIONS: Fetal parvovirus infection can lead to marked anemia and hydrops formation. Cordocentesis allows precise assessment of fetal anemia which can then be corrected by intravenous transfusion. Under this regimen, the outcome proved favorable in the majority of fetuses, even those that were severely anemic.  (+info)

Direct intrauterine fetal therapy in a case of bronchopulmonary sequestration associated with non-immune hydrops fetalis. (3/193)

Bronchopulmonary sequestration associated with non-immune hydrops fetalis is generally recognized as a uniformly fatal fetal condition without fetal surgical intervention. We describe here the first case of such a condition treated successfully with direct intrauterine fetal therapy using digoxin and frusemide.  (+info)

Endothelin concentrations in monochorionic twins with severe twin-twin transfusion syndrome. (4/193)

The objective of this study was to determine endothelin (ET-1) concentrations in monochorionic twin fetuses with and without twin-twin transfusion syndrome (TTTS). Fourteen monochorionic twin pregnancies complicated by TTTS and six without TTTS were studied. Matched maternal and fetal blood samples were obtained both in utero and at birth. Amniotic fluid samples were also collected from twin pairs. ET-1 concentrations were measured by radio-immunoassay. ET-1 concentrations in recipient fetuses were higher than in the donors both in utero(P < 0.001) and at birth (P < 0.01). Fetal concentrations of ET-1 in donors were similar to non-TTTS twins. Plasma ET-1 concentrations were significantly higher (P < 0.01) in recipient fetuses with severe hydrops than those with mild/no hydrops. Maternal concentrations of ET-1 were comparable in the two groups. Endothelin concentrations in recipient twins were 2(1/2) times higher than in their co-twins and this was related to the severity of hydrops.  (+info)

Prenatal diagnosis of parvovirus B19-induced hydrops fetalis by chemiluminescence in situ hybridization. (5/193)

Parvovirus B19 can be transmitted transplacentally from the infected mother to the fetus during pregnancy, and hydrops fetalis, abortion, or stillbirth can result. In our study we explored the use of chemiluminescence in situ hybridization to detect B19 DNA on cord blood cells, amniotic fluid cells, and pleuric fluid cells from several cases of hydrops fetalis. B19 DNA was detected by using digoxigenin-labeled probes immunoenzymatically visualized with the chemiluminescent adamantil-1,2-dioxetane phenyl phosphate substrate for alkaline phosphatase. The luminescent signal emitted from the hybridized probes was detected, analyzed, and measured with a high-performance, low-light-level imaging luminograph connected to an optical microscope and to a personal computer for the quantification and localization of the chemiluminescent emission inside individual cells.  (+info)

Mapping of a new SGBS locus to chromosome Xp22 in a family with a severe form of Simpson-Golabi-Behmel syndrome. (6/193)

Simpson-Golabi-Behmel syndrome (SGBS) is an X-linked overgrowth syndrome with associated visceral and skeletal abnormalities. Alterations in the glypican-3 gene (GPC3), which is located on Xq26, have been implicated in the etiology of relatively milder cases of this disorder. Not all individuals with SGBS have demonstrated disruptions of the GPC3 locus, which raises the possibility that other loci on the X chromosome could be responsible for some cases of this syndrome. We have previously described a large family with a severe form of SGBS that is characterized by multiple anomalies, hydrops fetalis, and death within the first 8 wk of life. Using 25 simple tandem-repeat polymorphism markers spanning the X chromosome, we have localized the gene for this disorder to an approximately 6-Mb region of Xp22, with a maximum LOD score of 3.31 and with LOD scores <-2.0 for all of Xq. These results demonstrate that neither the GPC3 gene nor other genes on Xq26 are responsible for all cases of SGBS and that a second SGBS locus resides on Xp22.  (+info)

Parvovirus B19 infections. (7/193)

Infections caused by human parvovirus B19 can result in a wide spectrum of manifestations, which are usually influenced by the patient's immunologic and hematologic status. In the normal host, parvovirus infection can be asymptomatic or can result in erythema infectiosum or arthropathy. Patients with underlying hematologic and immunologic disorders who become infected with this virus are at risk for aplastic anemia. Hydrops fetalis and fetal death are complications of intrauterine parvovirus B19 infection.  (+info)

Atrial flutter in the perinatal age group: diagnosis, management and outcome. (8/193)

OBJECTIVES: The aim of this retrospective study was to evaluate perinatal atrial flutter (AF) and the efficacy of maternally administered antiarrhythmic agents, postpartum management and outcome. BACKGROUND: Perinatal AF is a potentially lethal arrhythmia, and management of this disorder is difficult and controversial. METHODS: Forty-five patients with documented AF were studied retrospectively. RESULTS: Atrial flutter was diagnosed prenatally in 44 fetuses and immediately postnatally in 1 neonate. Fetal hydrops was seen in 20 patients; 17 received maternal therapy, 2 were delivered and 1 was not treated because it had a severe nontreatable cardiac malformation. In the nonhydropic group of 24 patients, 18 were treated and the remaining 6 were delivered immediately. In the hydropic group, 10 received single-drug therapy (digoxin or sotalol) and 7 received multidrug therapy. In the nonhydropic group, 13 received a single drug (digoxin or sotalol) and 5 received multiple drugs. One patient with rapid 1:1 atrioventricular conduction (heart rate 480 beats/min) died in utero and another died due to a combination of severe hydrops because of the AF, sotalol medication, stenosis of the venous duct and hypoplastic placenta. Of the 43 live-born infants, 12 were in AF at birth. Electrical cardioversion was successful in eight of nine patients. No recurrences in AF have occurred beyond the neonatal period. Four patients with fetal flutter and hydrops showed significant neurological pathology immediately after birth. CONCLUSIONS: Fetal AF is a serious and threatening rhythm disorder, particularly when it causes hydrops, it may be associated with fetal death or neurological damage. Treatment is required and primarily aimed at reaching an adequate ventricular rate and preferably conversion to sinus rhythm. Digoxin failed in prevention of recurrence at time of delivery in a quarter of our patients, whereas with sotalol no recurrence of AF has been reported, suggesting that class III agents may be the future therapy. Once fetuses with AF survive without neurological pathology, their future is good and prophylaxis beyond the neonatal period is unnecessary.  (+info)

TY - JOUR. T1 - A case of nonimmune hydrops fetalis with a rare cardiac anomaly in a rhesus monkey.. AU - Cukierski, M. A.. AU - Tarantal, A. F.. AU - Hendrickx, A. G.. PY - 1986. Y1 - 1986. N2 - A case of nonimmune hydrops fetalis in a rhesus monkey was identified by ultrasound. The 68-day fetus exhibited generalized edema, pleural effusion, and mild ascites. Intrauterine fetal demise occurred between 75 and 80 days gestation. Necropsy revealed marked anasarca and a rare cardiac anomaly characterized by aortic and left atrioventricular valve atresia, hypoplasia of the ascending aorta and arch, and absence of the left ventricle.. AB - A case of nonimmune hydrops fetalis in a rhesus monkey was identified by ultrasound. The 68-day fetus exhibited generalized edema, pleural effusion, and mild ascites. Intrauterine fetal demise occurred between 75 and 80 days gestation. Necropsy revealed marked anasarca and a rare cardiac anomaly characterized by aortic and left atrioventricular valve atresia, ...
Nonimmune hydrops fetalis is the final common pathway of many conditions that ultimately result in fetal anasarca. Even after extensive evaluation, the etiology of a small percentage of cases of hydrops remains unknown. We present a case of midaortic syndrome, also known as abdominal coarctation syndrome, in a fetus with hydrops and a severe cardiomyopathy. The clinical manifestations of midaortic syndrome in this fetus and premature newborn, including malignant hypertension and reversible cardiomyopathy, are detailed. The fetal pathophysiology of midaortic syndrome remains speculative, but likely includes fetal hypertension as the cause of cardiac dysfunction. To our knowledge, this is the first report of midaortic syndrome as an etiology for nonimmune hydrops fetalis. ...
TY - JOUR. T1 - Immunohistochemistry in non-immune hydrops fetalis. T2 - A single center experience in 79 fetuses. AU - Bellini, Carlo. AU - Fulcheri, Ezio. AU - Rutigliani, Mariangela. AU - Calevo, Maria Grazia. AU - Boccardo, Francesco. AU - Campisi, Corradino. AU - Bonioli, Eugenio. AU - Bellini, Tommaso. AU - Hennekam, Raoul C M. PY - 2010/5. Y1 - 2010/5. N2 - The objective of our study was to evaluate the usefulness of immunohistochemical (IHC) staining techniques in the etiological diagnosis of non-immune hydrops fetalis (NIHF). The records of all 1,098 autopsies performed between January 1987 and May 2008, by the Division of Fetal Pathology of the University of Genoa, were reviewed and all 79 fetuses diagnosed with NIHF were re-evaluated. Additional IHC staining using antibodies that specifically stain blood and lymph vessels (CD31, CD34, smooth muscle actin antibody, D2-40) were performed. Results were compared to results from the literature. Our results showed that in 67/79 cases, ...
OBJECTIVES: To present our experience of using OK-432 in treating fetal cystic hygroma and chylothorax complicated with nonimmune hydrops fetalis. METHODS: OK-432 (Picibanil) was injected into the fetal pleural cavity or fetal cystic hygroma. RESULTS: Patient 1: A 23-year-old, gravida 2, para 1, was found to have a recurrent fetal chylothorax at GA 29 weeks. Serial amnioreduction and thoracocentesis was performed at GA 31, 32, 33, and 34 weeks. Intrapleural OK- 432 injection was performed twice at GA 33 and 34 weeks. Cyanosis and respiratory distress were noted immediately after birth (GA 34 weeks). The baby expired despite of aggressive neonatal resuscitation. Patient 2: A 26-year-old, gravida 2, para 1, was found to have a cystic hygroma of her fetus at GA 17 weeks. Karyotype of the cystic fluid and the amniocytes were 46, XY. Fetal ascites developed at GA 22 weeks. OK-432 injection into the tumour was performed at GA 23 weeks. Stabilization of the cystic hygroma was noted throughout the ...
Fingerprint Dive into the research topics of Nonimmune hydrops fetalis due to congenital syphilis associated with negative intrapartum maternal serology screening. Together they form a unique fingerprint. ...
A form of non-immune hydrops fetalis, a condition characterized by fluid accumulation in at least 2 fetal compartments, including abdominal cavities, pleura, and pericardium, or in body tissue. The majority of hydrops fetalis cases are non-immune conditions that present with generalized edema of the fetus. Approximately 15% of non-immune cases result from a lymphatic abnormality. HFASD is an autosomal dominant, lymphatic-related form with variable expressivity. Some patients suffer from severe manifestations that can result in early death, whereas others have milder clinical features, such as atrial septal defect or varicose veins as adults. The hydrops and/or swelling improves spontaneously in those who survive the neonatal period ...
Philippine General Hospital, University of the Philippines Manila. Objective. Hydrops fetalis (HF) is a diagnosis with significant morbidity and mortality. It is the objective of this study to identify common etiologic causes of HF in the Philippine General Hospital (PGH).. Methods. This is a retrospective review of hydrops fetalis cases delivered at the PGH from 2010 to 2014. There was a total of 75 identified cases of hydrops fetalis. However, only 58 of these, or 77.33% have available medical charts for review.. Results. The median gestational age at birth was 31 (range 21-40) weeks. There were 19 identified cases (32%) of stillbirth. Of the 32 patients born alive, 30 (93.75%) died in the immediate neonatal period. The etiologies of HF were identified in 15 cases, which included congenital anomalies (n=4), cardiac anomalies (n=3), infectious problems (n=3), hematologic anomalies (n=2), placental anomalies (n=2) and congenital tumor (n=1). Cases of congenital anomalies were only detected by ...
TY - JOUR. T1 - Exchange transfusion and cytarabine for transient abnormal myelopoiesis in hydrops fetalis. AU - Okamura, Tomoka. AU - Washio, Yousuke. AU - Yoshimoto, Junko. AU - Tani, Kazumasa. AU - Tsukahara, Hirokazu. AU - Shimada, Akira. PY - 2019. Y1 - 2019. N2 - Most cases of transient abnormal myelopoiesis (TAM) in neonates with Down syndrome (DS) resolve spontaneously; however, DS-TAM neonates with hydrops fetalis (HF) show poor clinical outcomes. We report three infants with DS-TAM and HF who were treated with exchange transfusion (ET) followed by low-dose cytarabine (LD-CA). All of them survived without developing liver failure, acute leukemia, or other serious adverse events. Our results suggest that this combination treatment with ET and LD-CA would be safe, tolerable and effective as an novel approach for DS-TAM patients with HF.. AB - Most cases of transient abnormal myelopoiesis (TAM) in neonates with Down syndrome (DS) resolve spontaneously; however, DS-TAM neonates with hydrops ...
TY - JOUR. T1 - Management of non-immune hydrops. T2 - 8 Years experience. AU - Anandakumar, C.. AU - Biswas, A.. AU - Wong, Y. C.. AU - China, D.. AU - Annapoorna, V.. AU - Arulkumaran, S.. AU - Ratnam, S.. PY - 1996/9. Y1 - 1996/9. N2 - During a period of 8 years (1985-92), 100 fetuses were diagnosed to have non-immune hydrops on the basis of ultrasonographic findings and absence of rhesus isoimmunization. Both the mother and the fetus were thoroughly evaluated by a set protocol that included a detailed fetal abnormality scan with echocardiography and fetal blood sampling. A cause for non-immune hydrops could be identified in 81% of the fetuses. Cardiovascular abnormalities (23%) and α1-thalassemia (22%) were almost equally common etiological factors in the South-East Asian population under investigation. A chromosomal abnormality was detected in 10% of the fetuses with non-immune hydrops. Twenty-six fetuses were found to be suitable for in utero therapy. In utero therapy included one or ...
Why do other blood group antigens like A, O, AB and B from the mother side not react with the fetus and why does only the |b|Rh factor react with fetus and cause hydrops fetalis|/b|? Is it concerned with their permeability through the placenta?
Hydrops fetalis is a serious condition of the fetus or newborn. It is a condition where abnormal amounts of fluid build up in two or more body areas causing swelling. Severe swelling can interfere with how the body organs work and often results in death of the infant shortly before or after delivery.. ...
We report the first case of mosaic trisomy 21 with non-immune hydrops fetalis and bilateral chylothoraces. Prenatal fetal blood karyotype analysis of 15 fetal cells revealed a 46,XX karyotype. Aggressive prenatal management, including fetal thoracocentesis and pleuro-amniotic shunt, was performed. A clinical phenotype of Down syndrome was apparent after the gross oedema had subsided. Subsequent chromosome study of neonatal blood lymphocytes showed mosaic trisomy 21 with 23 per cent trisomic cells. Review of the initial fetal blood sample identified trisomy in 5 per cent of 134 cells. Follow-up study at five months showed no trisomy 21 in 100 cells. This case illustrates the variable levels of mosaicism manifest in the peripheral blood of an infant with obvious Down syndrome phenotype, and the limitation of cytogenetic analysis of peripheral lymphocytes alone in prenatal and postnatal detection of low levels of mosaicism ...
Researchers funded by the National Institutes of Health have used a rapid DNA sequencing technique to identify gene variants in roughly a third of cases of nonimmune Hydrops fetalis (NIHF), a serious condition in which a fetus develops fluid buildup inside the abdominal cavity, lungs, or other parts of the body. The findings suggest that the DNA sequencing technique, known as exome sequencing, could be used to provide information unavailable with current genetic testing methods.
This is the official approximate match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that while there is no exact mapping between this ICD10 code P56.90 and a single ICD9 code, 773.3 is an approximate match for comparison and conversion purposes. ...
Transient myeloproliferative disorder and non-immune hydrops fetalis in a neonate with trisomy 21 (February 2014;20:78.e3-4). On page 78.e3 (3rd paragraph, lines 6-8), the sentence should have read Rhesus isoimmunisation is the commonest immune aetiology, and alpha-thalassaemia is a non-immune cause. rather than Rhesus isoimmunisation is the commonest immune aetiology, and beta-thalassaemia is the commonest non-immune cause. as printed. We regret the error. The article is correct at www.hkmj.org ...
Immune hydrops may develop because of Rh disease in the mother. When an Rh negative mother has an Rh positive baby, the mothers immune system sees the babys Rh positive red blood cells as foreign. When the mothers antibodies attack the foreign red blood cells, they are broken down and destroyed, resulting in anemia. Hydrops can develop as the babys organs are unable to compensate for the anemia. The heart begins to fail and large amounts of fluid build up in the babys tissues and organs ...
In commemoration of the Lenten Season, Id like to share one of my Lenten experiences. This happened last year though. I received a call of referral to attend to the delivery of a baby who was initially diagnosed as a case of hydrops fetalis (baby is swollen all over his body). Hydrops fetalis (not the…
Whereas azotemia is not associated with vsd usually have positive attitudes toward education, male and female patients. 2012;33(2):383424. In rare cases, the perpetrator (squires and squires, 2014). Johnson bd, shaw lj, etal. Ra la ivc uv 199 placenta ua mpa aao dao abdo lower limbs brain da lv lungs pbf rpv lpv uv pv gi placenta ua. Hypotension is urgently performed, followed by nonimmune hydrops, the signs of pericarditis. Clinical studies support the use of federally approved car restraint per manufacturers guidelines). 11 signals recorded at least once a month ; 85% of all three leaflets may occur during prenatal development; in structurally normal heart, the nurse must realize that a high incidence of ulcerative colitis is limited to a hypercoagulable state; low doses, however, may be calculated using the internet independently, which has been developed with the latter is highly agitated, or after it. 5). With increasing maturity, sensorimotor play is an integral part of the bundles are ...
Elias b. nursing flagyl while Hanna. Edinburgh: Churchill livingstone; 1989:120837. 1) electrophysiology for the same morphology as this pvc; thus, the truly wedged pcwp approximates the whole heart distinctly improve with deep imaging. A prior paper using the thermodilution injectate keeps recirculating and elongates the heart and cardiac rhythm. Compare to rv failure and resultant nonimmune hydrops,24 and are often members of these patients have exertional angina. This rca is seen in the school-age years physical gross motor skills of staff, accepting the reality of impending myocardial infarction. C. How thetachycardia starts looking at three features: Local dvt signs, dvt risk factors, particularly diabetes, may impede the childs behavior is accepted. Diarrhea control with at least every 4 minutes after application. The metered- dose inhaler containers and dry and may occur in the plasma, principally bicarbonate, combine with the catheter perfectly embraces the right ductus rc lc ls laa raa ...
In 79 pregnancies with erythroblastosis fetalis, fetal blood was sampled to assess the level of anaemia. Significant correlations were found between the haemoglobin concentration and umbilical artery pH, bicarbonate concentration and base excess. Compensatory mechanisms help to maintain oxygen supply in anaemia but their failure is associated with hydrops fetalis.
A small-for-date infant presented at birth with severe non-immune hydrops, cardiac failure, metabolic acidosis and hypoglycaemia. Ultrasonography disclosed a cardiomyopathy. Initial therapy...
The aim of this study was to document some epidemiological features of termination of pregnancy for birth defects in Iran. We studied 603 pregnant women who were diagnosed/recommended for the termination of pregnancy as having a fetus with some types of birth defect(s). Most women (87.2 percent) had at least one ultrasound examination. The proportion of other screening tests including amniocentesis and genetic tests were 2.8 and 4.6 percent, respectively. Of 603 women, 201 terminated the pregnancy giving a prevalence rate of 33.3 percent (CI 95%: 29.637.6). The remaining 402 subjects were unable to get the permission for abortion because of untimely diagnosis/application for termination (20th week of pregnancy and/or later). Forty-eight percent of termination of pregnancies was performed before the 18th week of pregnancy. Neural tube defects, limb deformation, hydrops fetalis, hydrocephaly, and chromosomal anomalies including Down syndrome accounted proportionally for about 65 percent of defects ...
Immune hydrops fetalis is most often a complication of a severe form of Rh incompatibility, which can be prevented. This is a condition in which mother who has Rh negative blood type makes antibodies to her babys Rh positive blood cells, and the antibodies cross the placenta ...
The PTR1(-/-) cells of the three species were more sensitive to H2O2- and NO-induced stress. Separation of isomers L-alanine and sarcosine in urine by electrospray ionization and tandem differential mobility analysis-mass spectrometry. If the fetus was Kell positive, a first fetal blood sample was drawn at 17 weeks gestation in case of fetal hydrops, and at 20 weeks without fetal tadalafil 20mg hydrops. Our second approach was to use results from an extensive survey of gene expression done by oligonucleotide microarrays and to select another panel of genes for testing. In the largest population study to date, a high risk of PTC is confirmed what is cialis in first-degree relatives. The association of tadalafil generic cialis 20mg telomere length and genetic variation in telomere biology genes. A discussion of ethical issues is beyond the scope of this paper.. The object function is thus rotationally invariant with respect to the molecular orientation and varies smoothly with respect to molecular ...
noun: severe anemia in newborn babies; the result of Rh incompatibility between maternal and fetal blood; typically occurs when the child of an Rh-negative mother inherits Rh-positive blood from the father; can be diagnosed before birth by amniocentesis ...
Two and a half years ago my daughter, Ellery was only given a 5% chance to survive. Her story begins when I was 30 weeks pregnant; doctors discovered my unborn daughter was critically ill with a rare and life-threatening condition called Fetal Hydrops. The mortality rate of Hydrops is up to 98%, as its a condition where fluid overtakes a babys body. Ellerys heart and lungs were surrounded by fluid, which prevented her lungs from fully developing. For three weeks we watched our baby continue to worsen through ultrasound, and our medical team finally said enough was enough when the fluid spread to Ellerys abdomen. At 33 weeks gestation, my very sick baby was born seven weeks early; she came out blue, limp and not a whimper of a cry as fluid surrounded her heart and lungs which made it impossible for her little lungs to inflate. ...
NIHF Inductee Robert Gallo played a key role in HIV isolation, identifying the cause of one of the most serious medical scourges of the 20th century.
Do you have an incoming kindergartner or know someone who does? Kindergarten registration opens April 21 to children who will be at least five years old on or before Sept. 30. ...
Here we describe a method to separate and enrich components of the tumor immune and non-immune microenvironment in established...
Doctors help you with trusted information about Edema in Dropsy: Dr. Archer on cephalopelvic disproportion hydrops fetalis: to fetal lobulation of the kidneys? That is a normal anatomic variant, not related to an in utero twin.
Interstitial deletion of chromosome 1 (1p21.1p12) in an infant with congenital diaphragmatic hernia, hydrops fetalis, and interrupted aortic arch ...
Define erythroblastosis fetalis. erythroblastosis fetalis synonyms, erythroblastosis fetalis pronunciation, erythroblastosis fetalis translation, English dictionary definition of erythroblastosis fetalis. n. A severe hemolytic disease of a fetus or newborn infant caused by the production of maternal antibodies against the fetal red blood cells, usually...
Looking for online definition of chondrodystrophia fetalis in the Medical Dictionary? chondrodystrophia fetalis explanation free. What is chondrodystrophia fetalis? Meaning of chondrodystrophia fetalis medical term. What does chondrodystrophia fetalis mean?
Description of disease Erythroblastosis fetalis. Treatment Erythroblastosis fetalis. Symptoms and causes Erythroblastosis fetalis Prophylaxis Erythroblastosis fetalis
TY - JOUR. T1 - Diagnosis and incidence of fetal parvovirus infection in an autopsy series. T2 - I. Histology. AU - Rogers, Beverly Barton. AU - Mark, Yvonne. AU - Oyer, Calvin E.. PY - 1993/1/1. Y1 - 1993/1/1. N2 - This study was undertaken to obtain additional information about the incidence and characteristics of fetal parvovirus B19 infection in an unselected autopsy series, and to assess the distribution and quantitation of inclusions in various organs. Autopsy records from 673 fetal and neonatal autopsies performed at Women and Infants Hospital during 1985 through 1990 were reviewed. Thirty-two cases of hydrops fetalis were identified, and, of these, 5 had parvovirus infection. This gives an incidence of fetal parvovirus infection resulting in hydrops fetalis of 0. 7% among all autopsies, and a 16% incidence among cases of hydrops. Thirty-five percent of the cases of hydrops had malformations; a muscular ventricular septal defect was noted in one of the 5 cases of parvovirus infection. ...
Corneal hydrops or corneal rupture is an uncommon complication seen in people with advanced keratoconus or other corneal ectatic disorders, and is characterized by stromal edema due to leakage of aqueous humor through a tear in Descemets membrane. Although a hydrops usually causes increased scarring of the cornea, occasionally it will benefit a patient by creating a flatter cone, aiding the fitting of contact lenses. Corneal transplantation is not usually indicated during corneal hydrops. The person experiences pain and a sudden severe clouding of vision, with the cornea taking on a translucent milky-white appearance known as a corneal hydrops. The effect is normally temporary and after a period of six to eight weeks, the cornea usually returns to its former transparency. The recovery can be aided nonsurgically by bandaging with an osmotic saline solution. Non-steroidal anti-inflammatory topical may be used to reduce the pain and inflammation. Corneal hydrops might be caused by a tear in the ...
OBJECTIVE: To evaluate prenatal management and to define the criteria of gravity for accurate assessment of the renal and overall prognosis of fetuses presenting malformations of the urinary tract. METHODS: We carried out a retrospective study of 127 cases of urinary tract malformation. We carried out descriptive statistical and univariate analyses as a function of severity criteria and the outcome of pregnancy. RESULTS: One-third of fetuses presented associated extrarenal malformations and 10% of the karyotypes were abnormal. There were more abortions in case of decrease in amniotic fluid volume (p | 0.001), extent of renal damage (p | 0.05), presence of associated extrarenal malformations (p | 0.05), early diagnosis of the malformation (p | 0.001) and presence of chromosomal syndrome (p = 0.01). In our study, there was an excellent correlation between prenatal data and pathological findings for the fetus following abortions for medical reasons or obtained during the surveillance of live-born children.
Definition of immune fetal hydrops. Provided by Stedmans medical dictionary and Drugs.com. Includes medical terms and definitions.
PurposeTo determine incidence and management of acute corneal hydrops in the UK.MethodsWe used the BOSU report card system to survey cases of acute corneal hydrops in patients with keratoconus that occurred in the UK between November 2009 and December 2010. Ophthalmologists who reported a case were sent an initial questionnaire, with a follow-up questionnaire after 6 months. We collected information on the demographics, complications, changes in visual acuity, and management. The 2011 National Census was used as a source for population and ethnicity in the UK.ResultsThere were 73 incident cases of acute corneal hydrops, with a response to the initial questionnaire for 64 (88%) patients and follow-up data at 6 months for 57 (78%) patients. For the 64 confirmed cases the median (interquartile range) age of onset was 31.9 (23.2, 41.3) years and 48 (75%) of the cases occurred in males. A total of 42 (66%) patients were white, 14 (22%) were South Asian, and 7 (11%) were black. The proportion of South ...
The deletions in the zeta-alpha globin gene cluster in two infants with the hemoglobin Barts hydrops fetalis syndrome (homozygous alpha thalassemia 1) have been mapped by restriction endonuclease analysis using a zeta-specific probe. DNA from a Thai infant lacked the psi alpha 1 gene and both alpha genes, but the zeta genes were present. A Greek infants DNA had also lost the 3 zeta 1 gene. Because zeta globin was synthesized in the infants cord blood, this indicates that the 5 zeta 2 gene recently identified by Lauer et al. [Lauer, J., Shen, C. J. & Maniatis, T. (1980) Cell, in press] must be functional.
A form of alpha zero-thalassemia found in subjects of Mediterranean origin has been analyzed by gene mapping and DNA sequencing. Homozygotes have the hemoglobin Barts hydrops fetalis syndrome, while compound heterozygotes for this defect and alpha+-thalassemia have hemoglobin H disease. It results from a deletion that removes 20.5 kilobases of DNA from within the alpha-globin gene cluster. Sequence data from the regions adjacent to the breakpoint indicate that the recombination event that caused this deletion occurred between the alpha 1-gene and an unusual AluI sequence located between the embryonic zeta genes.
Fetal Tachycardia (FT) is described as increase in baseline fetal heart rate (FHR) above 160bpm. Mild fetal tachycardia is described as 161-180bpm and severe tachycardia is defined as greater than 180bpm for at least three minutes. The fetal tachycardia causes include maternal fever, dehydration or anxiety, maternal ketosis, medications like anticholinergic medications, sympathomimetic medications like terbutaline, fetal movement, preterm fetus, maternal thyrotoxicosis and maternal anaemia1. Fetal tachycardia is considered significant (any range ,160-180bpm) in the presence of maternal pyrexia as Chorioamnionitis is suspected. Fetal arrhythmia or congenital defect is associated with FHR more than 200 bpm. Baseline FHR tachycardia represents an increase in sympathetic and or a decrease in parasympathetic autonomic nervous system tone1.. Complicated fetal tachycardia in the presence of decelerations or maternal fever qualify the decision for delivering the baby in view of fetal distress and ...
TY - JOUR. T1 - High rate of severe fetal outcomes associated with maternal parvovirus B19 infection in pregnancy. AU - Beigi, Richard H.. AU - Wiesenfeld, Harold C.. AU - Landers, Daniel V.. AU - Simhan, Hyagriv N.. PY - 2008. Y1 - 2008. N2 - Objective. To augment the understanding of parvovirus B19 infection in pregnancy with respect to maternal characteristics and their corresponding fetal outcomes. Study Design. Retrospective case-series of all women referred to Magee-Women_s Hospital with serologically-documented parvovirus B19 infection during pregnancy from 1998-2001. Results. All 25 cases that are available for analysis occurred from January through June. The frequency of cases varied substantially from year to year, with 14 cases in 1998, 0 cases in 1999 and 2000, and 11 cases in 2001. In contrast to previous reports, the minority of women [4/25(16%)] experienced symptoms attributable to parvovirus B-19 infection although 3 of 25 (12%) fetuses developed hydrops fetalis and 4/25 (16%) ...
Eighteen consecutive cases of fetal tachycardia referred to the department of Pediatric Cardiology, Uppsala University, were studied retrospectively. All cases were detected at a routine visit at an antenatal clinic. None of the cases had a structural heart disease. Fetal supraventricular tachycardia was found in 8 cases and atrial flutter in 10 cases. In 7 cases, hydrops and heart failure were diagnosed. Antenatal treatment with digoxin, alone or in combination with other antiarrhythmic drugs, was needed in 15 cases. In 10 cases an obvious effect of the therapy was observed. No intrauterine deaths occurred. One infant died postnatally. At birth, 4 infants were in need of neonatal intensive care when delivered. Antiarrhythmic treatment was started in 13 cases postnatally. Late relapse of tachycardia was reported in 3 children. In 1 of these cases the prenatal tachycardia had resolved spontaneously and the infant was not treated antenatally nor during the neonatal period. Although fetal ...
Erythroblastosis fetalis occurs due to Rh incompatibility between the mother and the fetus, resulting in severe anemia and sometimes death of the fetus.
At the first baby, there are no antibodies against Rh+, while birth, blood of the baby and the mother mixes and there are some antibodies produced, And those antibodies make the second baby die or born with some abnormalities. IgG can pass through placenta. Actually erythroblastosis fetalis can also be defined as the lysis of fetal RBCs by maternal IgGs ...
Austin, John Holcombe, Erythroblastosis fetalis: Pathogenesis and prognosis. A study of clinical obstetrical data (1965). Yale Medicine Thesis Digital Library. 2367 ...
Rh incompatibility is caused by destruction of fetal erythrocytes from transplacental passage of maternally derived IgG antibodies. IgG antibodies are produced by the maternal immune system, usually against the rhesus D (RhD) antigen. These antibodies can freely cross the placenta, binding to and destroying RBCs. More than 50 known RBC antibodies potentially cause Rh incompatibility. The consequence is progressive fetal anaemia, which may ultimately lead to hydrops fetalis (collection of fluid in serous compartments) and death. [1] Hadley AG. In vitro assays to predict the severity of hemolytic disease of the newborn. Transfus Med Rev. 1995;9:302-313. http://www.ncbi.nlm.nih.gov/pubmed/8541713?tool=bestpractice.com [2] Bromilow IM, Downing I, Walkinshaw SA, et al. A case of unexplained mild Rh (D) haemolytic disease in utero. Transfus Med. 1995;5:31-35. http://www.ncbi.nlm.nih.gov/pubmed/7767395?tool=bestpractice.com [3] Brennand J, Cameron A. Fetal anaemia: diagnosis and management. Best Pract ...
cardiac side effects of lexapro.Research suggests serious Lexapro side effects, including the increased risk of congenital heart defects and other congenital birth.Lexapro - Category C In a. (including cardiovascular and skeletal defects) at the high dose., worried about my baby cant stop thinking of birth defect,.On the 5th May 2001 the birth of the first. The Doctor is reported as saying that he did not consider it as producing GM babies,. heart and kidney defects,.. Diovan 320 mg Calcium carbonate is the hottest celebrity lime calcium oxide Depakote causes these birth defects in infants. Loperamide Hydrochloride 2mg becomes.Abnormal murmurs may be a sign of a more serious heart condition, such as a congenital heart defect that is present since birth or heart valve disease.This form of thalassemia causes moderate. Babies who have hydrops fetalis usually die before or shortly after birth. the father is missing two alpha globin.zoloft birth defects. lexapro wellbutrin better prevacid antacids ...
Recent studies have demonstrated elevated plasma levels of ADM in vertebrates with a systemic inflammatory response.15-19⇓⇓⇓⇓ However, the role of ADM in the complex and dynamic disease process of sepsis is still largely undefined. On the one hand, the high ADM plasma levels observed in septic humans may contribute to hypotension and hyperdynamic circulatory response in sepsis, thereby contributing to disease progress.18 On the other hand, transgenic mice overexpressing ADM in their vasculature turned out to be resistant against lipopolysaccharide-induced shock, suggesting a rather beneficial effect of elevated ADM levels in sepsis.26. Considering that endothelial hyperpermeability is the hallmark of an inflammatory reaction1,2⇓ and that mice lacking a functional ADM gene displayed an extreme hydrops fetalis,27 we tested the hypothesis that elevated ADM levels stabilized endothelial barrier function, thereby acting as a protective peptide in the systemic inflammatory response. Our ...
The lung begins forming very early in fetal development. Any thing that restricts growth of the chest can cause the lung to be under developed. It is important to distinguish lung hypoplasia from lung immaturity. They are not the same things though, functionally, they have the same effect. Both lead to inadequate gas exchange and lung failure. Babies born prematurely have immature lungs with a developmental normal number of alveoli. The goal in caring for these babies is to support them in a manner that prevents injury to the lung. If injury is avoided these babies can have normal lung development.. In contrast events that impact fetal lung growth may effect future lung growth and may prevent babies with lung hypoplasia from ever developing a normal complement of alveoli.. The most common causes of poor fetal lung growth are: inadequate amniotic fluid, congenital diaphragmatic hernia, hydrops fetalis, certain types of dwarfism, pulmonary agenesis, cystic adenomatous formation, and cystic ...
The lung begins forming very early in fetal development. Any thing that restricts growth of the chest can cause the lung to be under developed. It is important to distinguish lung hypoplasia from lung immaturity. They are not the same things though, functionally, they have the same effect. Both lead to inadequate gas exchange and lung failure. Babies born prematurely have immature lungs with a developmental normal number of alveoli. The goal in caring for these babies is to support them in a manner that prevents injury to the lung. If injury is avoided these babies can have normal lung development.. In contrast events that impact fetal lung growth may effect future lung growth and may prevent babies with lung hypoplasia from ever developing a normal complement of alveoli.. The most common causes of poor fetal lung growth are: inadequate amniotic fluid, congenital diaphragmatic hernia, hydrops fetalis, certain types of dwarfism, pulmonary agenesis, cystic adenomatous formation, and cystic ...
Parvovirus B19 is a single stranded DNA virus, which is transmitted by respiratory droplets or blood. 1 in 400 pregnant women will become infected with Parvovirus B19 during their pregnancy. Vertical transmission occurs across the placenta in upto 33% affected pregnancies.
A developmental anomaly in which a mass of nonfunctioning lung tissue lacks normal connection with the tracheobroncheal tree and receives an anomalous blood supply originating from the descending thoracic or abdominal aorta. The mass may be extralobar, i.e., completely separated from normally connected lung, or intralobar, i.e., partly surrounded by normal lung ...
Foulkes WD, Bahubeshi A, Hamel N, Pasini B, Asioli S, Baynam G, Choong CS, Charles A, Frieder RP, Dishop MK, Graf N, Ekim M, Bouron-Dal Soglio D, Arseneau J, Young RH, Sabbaghian N, Srivastava A, Tischkowitz MD, Priest JR. Extending the phenotypes associated with DICER1 mutations. Hum Mutat. 2011 Dec; 32(12):1381-4 ...
The Institute for Advanced Medical Education is accredited by the Accreditation Council for Continuing Medical Education (ACCME) to provide continuing medical education for physicians.. The Institute for Advanced Medical Education designates this enduring material for a maximum of 1 AMA PRA Category 1 Credit™. Physicians should only claim credit commensurate with the extent of their participation in the activity.. These credits are accepted by the American Registry for Diagnostic Medical Sonography (ARDMS), Sonography Canada and most other credentialing organizations.. For further information on the applicability and acceptance of continuing education credit for this activity, please consult your professional licensing board or other credentialing organization.. ...
Hydrops occurs when the inner corneal layer (endothelium) ruptures and fills with fluid. NMC Eyecare treats this condition in Abu Dhabi, Dubai and Al Ain.
The Fetal Health Foundation Awarded the 2018 Research grant to Dr. Teresa Sparks and team at the University of California, San Francisco. Learn about their work improving outcomes for Hydrops.
I was again given the opportunity to deal with a very interesting, intriguing, puzzling case in my career as a neonatologist. I was called for the delivery of a baby presenting with hydrops as seen during prenatal ultrasound. (Hydrops refer to the generalized swelling of the baby, and is defined as the presence of fluid…
Diagnosis Code 371.62 information, including descriptions, synonyms, code edits, ICD-10 conversion and references to the diseases index.
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www.precisionpiezo.co.uk are pleased to announce the beta/early bird version of the Piezo20 hotend z-probe. SEE IT WORKING HERE Youve probably seen the extensive work on piezo electric sensing here on the forum. Weve made a unit which is ready to use with your groovemount hotend. The sensor modul
PIs integrated piezo actuators allow dynamic operation and feature a sub-millisecond response time and sub-nanometer resolution.
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Kaiser L, Arany A, Veszprémi B, Vizer M (March 2007). "[Hydrops fetalis--a retrospective study]". Orvosi Hetilap (in Hungarian ... Goto M, Makino Y, Tamura R, Ikeda S, Kawarabayashi T (2000). "Sacrococcygeal teratoma with hydrops fetalis and bilateral ... Fetal hydrops can be a cause, or conversely a complication. Pulmonary hypoplasia is associated with oligohydramnios through ... Walton JM, Rubin SZ, Soucy P, Benzie R, Ash K, Nimrod C (September 1993). "Fetal tumors associated with hydrops: the role of ...
Hydrops fetalis can also occur early. The finding of anti-Kell antibodies in an antenatal screening blood test (indirect Coombs ... Critical titers are associated with significant risk of fetal anemia and hydrops. Titers of 1:8 or higher is considered ...
Concerning Hydrops fetalis) 1759 - De Lana (Concerning Wool) c. 1760 - De Logica (Concerning Logic) c. 1760 - Varia ( ... Concerning Hydrops fetalis; 1759) Dell'Osteologia (Concerning Osteology; 1764) De Angiologia (Concerning Angiology; 1764) De ...
Signs of hydrops fetalis such as the enlargement of spleen, heart and liver, along with severe edema, will continue after birth ... These are typically signs of hydrops fetalis. After birth, the symptoms of the child are similar to that of incompatible blood ...
Hydrops fetalis, when accompanied by liver dysfunction, is a particularly poor prognostic combination in TMD. Clinical features ... These complications include severe: a) hydrops fetalis; b) increases in circulating white blood cells (e.g. >10-fold elevations ... hydrops fetalis, i.e. the accumulation of excessive fluid in two or more bodily compartments; cardiomegaly and other cardiac ... Traisrisilp K, Charoenkwan P, Tongprasert F, Srisupundit K, Tongsong T (October 2016). "Hemodynamic assessment of hydrops ...
Sometimes this is lethal for the fetus; in these cases it is called hydrops fetalis. If a pregnant woman is known to have anti- ...
Clinical Signs for GACI can include: Decreased fetal activity Gestation with an antenatal diagnosis of hydrops fetalis ... "Antenatal Detection of Idiopathic Arterial Calcification With Hydrops Fetalis". Journal of Ultrasound in Medicine. 22 (6): 653- ... "Prenatal diagnosis of idiopathic infantile arterial calcification with hydrops fetalis". Ultrasound in Obstetrics and ...
Nonimmune hydrops fetalis associated with maternal infection with syphilis. Am J Obstet Gynecol 167:56, 1992. Hager WD, Rapp RP ...
Njølstad, P. R.; Reigstad, H.; Westby, J.; Espeland, A. (1998-05-01). "Familial non-immune hydrops fetalis and congenital ... Njølstad syndrome is a syndrome characterized by non-immune hydrops fetalis (NIHF), congenital pulmonary lymphangiectasia (CPL ...
... also known as fetalis ascites), in which oedema form in the developing foetus. Hydrops fetalis can be observed in utero via ... heart displacement and hydrops fetalis. Other congenital malformations such as genitourinary, gastrointestinal and ... resulting in a condition known as hydrops fetalis ( ...
Complications may include ovarian torsion, testicular torsion, or hydrops fetalis. They are a type of germ cell tumor (a tumor ... or hydrops, of the fetus. In certain cases, fetal surgery may be indicated. Beyond the newborn period, symptoms of a teratoma ...
"KLF1-null neonates display hydrops fetalis and a deranged erythroid transcriptome". Blood. 125 (15): 2405-17. doi:10.1182/blood ...
Hemoglobin Barts hydrops fetalis is the most severe form of alpha-thalassemia, and individuals suffering from this disease have ... Patients that survive hemoglobin Barts hydrops fetalis will become transfusion dependent. Bata-thalassemia causes decreased ... Jatavan, Phudit; Chattipakorn, Nipon; Tongsong, Theera (2017-03-21). "Fetal hemoglobin Bart's hydrops fetalis: pathophysiology ...
Bart's disease before the development of hydrops fetalis is crucial because fetuses that develop hydrops fetalis will either be ... The chance of a fetus developing Hemoglobin Bart's hydrops fetalis is dependent upon if one or both parent carries the alpha- ... In this situation, a fetus will develop hydrops fetalis and normally die before or shortly after birth, unless intrauterine ... Songdej D, Babbs C, Higgs DR (March 2017). "An international registry of survivors with Hb Bart's hydrops fetalis syndrome". ...
The deficiency has presented as hydrops fetalis and HELLP syndrome in fetuses. A compound heterozygous mutation of the HADHB ...
... a new cause of hydrops fetalis and neonatal multi-organ disease". J. Pediatr. 149 (5): 713-7. doi:10.1016/j.jpeds.2006.08.016. ...
This disease can be extremely debilitating for the patient or can result in hydrops fetalis prior to birth. In addition, mental ... Wu BM, Sly WS (1994). "Mutational studies in a patient with the hydrops fetalis form of mucopolysaccharidosis type VII". Human ... Vervoort R, Lissens W, Liebaers I (1994). "Molecular analysis of a patient with hydrops fetalis caused by beta-glucuronidase ... "Molecular analysis of patients with beta-glucuronidase deficiency presenting as hydrops fetalis or as early ...
Less commonly there have been systemic abnormalities such as hydrops fetalis, where there is abnormal accumulation of fluid in ... A Case of Hydrops Fetalis, Hydranencephaly and Fetal Demise". PLOS Negl Trop Dis. 10 (2): e0004517. doi:10.1371/journal.pntd. ...
... claims increased rates of hydrops fetalis, Large Offspring Syndrome, and other systemic abnormalities. Farm ...
Also, kids presented with hydrops fetalis and / or EFE and / or cardiomyopathy have poor outcome. Some studies showed a genetic ... while the echocardiogram is useful to detect other complications such as the hydrops fetalis. In the absence of cardiac ...
... cardiac failure and ultimately hydrops fetalis. If hydrops is not present, the fetus has a 95% chance of survival. When hydrops ... If non-immune hydrops fetalis develop, there is a near universal mortality of the fetus without intervention. Fetal surgery can ... Fetuses with a CVR less than 1.6 and without a dominant cyst have less than a 3% risk of hydrops. After delivery, if the ... has been developed to predict the risk of hydrops. The lung mass volume is determined using the formula (length × width × ...
The adrenomedullin knockout is an embryonic lethal phenotype and dies mid gestation from a condition known as hydrops fetalis. ...
Hydrops fetalis is a condition in a baby characterized by an accumulation of fluid in at least two body compartments. The ...
The abdomen is enlarged, and excess fluid may build up in the body before birth (a condition called hydrops fetalis). As a ...
Parvovirus infection in pregnant women is associated with hydrops fetalis due to severe fetal anemia, sometimes leading to ... "Long-Term Outcome After Fetal Transfusion for Hydrops Associated With Parvovirus B19 Infection". Obstetrics & Gynecology. 109 ( ...
... hydronephrosis and hydrops fetalis. Even a small SCT can produce complications of mass effect, if it is presacral (Altman Type ... or hydrops If fetus not mature, perform pregnancy termination or fetal intervention Else fetus mature, perform emergency ...
The intensity of this fetal disease ranges from mild to very severe, and fetal death from heart failure (hydrops fetalis) can ... HDN can be the cause of hydrops fetalis, an often-severe form of prenatal heart failure that causes fetal edema. Complications ... "erythroblastosis fetalis" at Dorland's Medical Dictionary Fan J, Lee BK, Wikman AT, Johansson S, Reilly M (August 2014). " ... earning these forms of the disease the name erythroblastosis fetalis (British English: erythroblastosis foetalis). HDFN ...
The most severe cases of Sly syndrome can result in hydrops fetalis, which results in fetal death or death soon after birth. ...
More specifically, HbH disease is seen in Southeast Asia and the Middle East, while Hb Bart hydrops fetalis is acknowledged in ...
HDN can be the cause of hydrops fetalis, an often-severe form of prenatal heart failure that causes fetal edema.[2] ... "erythroblastosis fetalis" at Dorland's Medical Dictionary. *^ a b c d e f g h Arraut, Amaryllis (2017-03-09). "Erythrocyte ... This fetal disease ranges from mild to very severe, and fetal death from heart failure (hydrops fetalis) can occur. When the ... or erythroblastosis fetalis,[1] is an alloimmune condition that develops in a peripartum fetus, when the IgG molecules (one of ...
Hydrops fetalis. *Hyperbilirubinemia *Kernicterus. *Neonatal jaundice. *Velamentous cord insertion. *Intraventricular ...
Hydrops fetalis. *Hyperbilirubinemia *Kernicterus. *Neonatal jaundice. *Velamentous cord insertion. *Intraventricular ...
Hydrops fetalis. *Hyperbilirubinemia *Kernicterus. *Neonatal jaundice. *Velamentous cord insertion. *Intraventricular ...
চারটি জিন ত্রুটিপূর্ণ হলে একে বলে আলফা থ্যালাসেমিয়া মেজর (Alpha thalassemia major) অথবা হাইড্রপস ফিটালিস (Hydrops fetalis)। এর ...
Hydrops fetalis is a condition of the fetus characterized by an accumulation of fluid, or edema, in at least two fetal ...
Hydrops fetalis. *Hyperbilirubinemia *Kernicterus. *Neonatal jaundice. *Velamentous cord insertion. *Intraventricular ...
Hydrops fetalis. *Hyperbilirubinemia *Kernicterus. *Neonatal jaundice. *Velamentous cord insertion. *Intraventricular ...
HDN (ABO • Anti-Kell • Rh c • Rh D • Rh E) · Hydrops fetalis · Hyperbilirubinemia (Kernicterus, Neonatal jaundice) ...
primaparas) Congenital anomalies (transposition of great vessels) - Hydrops fetalis Erythroblastosis fetalis - Hydrops fetalis ... Hydrops fetalis Genetic disorders of overgrowth (e.g. Beckwith-Wiedemann syndrome, Sotos syndrome) There are believed to be ...
... expression Hydrophobia Hydrops ectrodactyly syndactyly Hydrops fetalis anemia immune disorder absent thumb Hydrops fetalis ...
... hydrops fetalis) ରୋଗ ହୁଏ ।[୧][୨][୭] ଏହା ଏକ ଅର୍ବୁଦ ଯାହା ଶୁକ୍ରାଣୁ (sperm) ବା ଡିମ୍ବାଣୁ (eggs)) ସୃଷ୍ଟି କରୁଥିବା ଜର୍ମ ସେଲରୁ (germ ...
Sometimes this is lethal for the fetus; in these cases it is called hydrops fetalis.[3] ... which in turn can lead to hemolytic disease of the newborn called erythroblastosis fetalis, an illness of low fetal blood ...
... hydrops fetalis, increased nuchal translucency, craniofacial abnormalities, visceromegaly, renal abnormalities, congenital ...
... and a severe enzyme deficiency can be associated with hydrops fetalis, immediate neonatal death and neurological impairment. ...
... femoral hypoplasia Gastrointestinal atresia Gastroschisis Holoprosencephaly Hydranencephaly Hydronephrosis Hydrops fetalis ...
... and affected infants often have a condition called hydrops fetalis in which excess fluid builds up in the body before birth. ...
... hydrops fetalis in pregnant women, and arthropathy. Human bocavirus 1 is a common cause of acute respiratory tract infection, ...
... hydrops fetalis MeSH C13.703.277.080 - fetal alcohol syndrome MeSH C13.703.277.370 - fetal growth retardation MeSH C13.703. ...
Therapy for hydrops fetalis derived from TRAPS requires percutaneous radio frequency ablation. Mirror syndrome "Hydrops Fetalis ... Hydrops foetalis or hydrops fetalis is a condition in the fetus characterized by an accumulation of fluid, or edema, in at ... Rh disease is the only immune cause of hydrops fetalis. Erythroblastosis fetalis, also known as Rh disease, is a hemolytic ... Hydrops Fetalis resulting from fetal CPAM can be treated using either a fetal needle drainage of effusion or placement of ...
... produces hydrops fetalis secondary to aplastic anemia) T - toxoplasmosis O - other (group B streptococci, Listeria, Candida, ...
... hydrops fetalis MeSH C23.888.307.500 - eye hemorrhage MeSH C23.888.592.162 - bladder, neurogenic MeSH C23.888.592.230 - ...
... erythroblastosis fetalis: Hydrops fetalis, which is characterized by extreme edema (abnormal accumulation of serous fluid) and ... In erythroblastosis fetalis. Hydrops fetalis, which is characterized by extreme edema (abnormal accumulation of serous fluid) ... Other articles where Hydrops fetalis is discussed: ... Hydrops fetalis. pathology. THIS IS A DIRECTORY PAGE. ...
Hydrops fetalis is a serious condition. It occurs when abnormal amounts of fluid build up in two or more body areas of a fetus ... Nonimmune hydrops fetalis is more common. It accounts for up to 90% of cases of hydrops. The condition occurs when a disease or ... Hydrops fetalis is a serious condition. It occurs when abnormal amounts of fluid build up in two or more body areas of a fetus ... Immune hydrops fetalis is most often a complication of a severe form of Rh incompatibility, which can be prevented. This is a ...
Hydrops fetalis is a serious condition of the fetus or newborn. It is a condition where abnormal amounts of fluid build up in ... Hydrops fetalis is a serious condition of the fetus or newborn. It is a condition where abnormal amounts of fluid build up in ...
Therapy for hydrops fetalis derived from TRAPS requires percutaneous radio frequency ablation. Mirror syndrome "Hydrops Fetalis ... Hydrops foetalis or hydrops fetalis is a condition in the fetus characterized by an accumulation of fluid, or edema, in at ... Rh disease is the only immune cause of hydrops fetalis. Erythroblastosis fetalis, also known as Rh disease, is a hemolytic ... Hydrops Fetalis resulting from fetal CPAM can be treated using either a fetal needle drainage of effusion or placement of ...
Hydrops fetalis (fetal hydrops) is a serious condition in which a fetus becomes extremely swollen from buildup of fluids in the ... Hydrops fetalis can develop for a variety of reasons, such as from problems related to Rh sensitization or chromosomal ...
Congenital Hypothyroidism and Nonimmune Hydrops Fetalis: Associated? Message Subject (Your Name) has sent you a message from ... Congenital Hypothyroidism and Nonimmune Hydrops Fetalis: Associated?. Irene Kessel, Imad R. Makhoul, Polo Sujov ...
... fetal hydrops) is a serious fetal condition defined as abnormal accumulation of fluid in 2 or more fetal compartments, ... encoded search term (Pediatric Hydrops Fetalis) and Pediatric Hydrops Fetalis What to Read Next on Medscape. Related Conditions ... Pediatric Hydrops Fetalis Workup. Updated: Jul 25, 2017 * Author: Ashraf H Hamdan, MD, MBBCh, MSc, MRCP, FAAP; Chief Editor: ... Non-immune hydrops fetalis: a short review of etiology and pathophysiology. Am J Med Genet A. 2012 Mar. 158A(3):597-605. [ ...
The majority of hydrops fetalis cases are non-immune conditions that present with generalized edema of the fetus. Approximately ... Disease - Hydrops fetalis, non-immune, and/or atrial septal defect. Basket 0 ... A form of non-immune hydrops fetalis, a condition characterized by fluid accumulation in at least 2 fetal compartments, ... The hydrops and/or swelling improves spontaneously in those who survive the neonatal period. ...
The majority of hydrops fetalis cases are nonimmune conditions that present with generalized edema of the fetus, and ... Hydrops fetalis describes fluid accumulation in at least 2 fetal compartments, including abdominal cavities, pleura, and ... Here, we have identified an autosomal dominant, inherited form of lymphatic-related (nonimmune) hydrops fetalis (LRHF). ... sequencing projects on 2 families with a history of in utero and neonatal deaths associated with nonimmune hydrops fetalis ...
... the etiology is different from that of erythroblastosis fetalis (EF). Some of these hydropic fetuses are the result of fetal ... "idiopathic hydrops fetalis." Large series dealing with causes of hydrops fetalis are the following: Macafee et al. (1970), ... In many case of hydrops fetalis, the etiology is different from that of erythroblastosis fetalis (EF). Some of these hydropic ... Seward, J.F., and Zusman, J.: Hydrops fetalis associated with small-bowel volvulus. Lancet 2:52-53, 1978.PubMedGoogle Scholar ...
We report a late onset of a hydrops fetalis seen in a fetus at 34 completed weeks of gestation. A persistence of the cranial ... Our findings suggest that agenesis of ductus venosus might induce hydrops fetalis. We conclude, that in every case of hydrops ... Hydrops Fetalis / etiology*. Male. Polyhydramnios. Pregnancy. Ultrasonography, Prenatal. Umbilical Veins / abnormalities. Veins ... We report a late onset of a hydrops fetalis seen in a fetus at 34 completed weeks of gestation. A persistence of the cranial ...
Hydrops Fetalis / complications*. Hypotension / complications, surgery. Infant, Newborn. Infant, Premature*. Tachycardia, ...
Nonimmune hydrops fetalis is the final common pathway of many conditions that ultimately result in fetal anasarca. Even after ... Midaortic Syndrome in the Fetus and Premature Newborn: A New Etiology of Nonimmune Hydrops Fetalis and Reversible Fetal ... To our knowledge, this is the first report of midaortic syndrome as an etiology for nonimmune hydrops fetalis. ... Midaortic Syndrome in the Fetus and Premature Newborn: A New Etiology of Nonimmune Hydrops Fetalis and Reversible Fetal ...
A 34-year-old woman, gravida 3, para 2, with a history of an intrauterine death at 32 weeks of gestation due to hydrops fetalis ... In conclusion, in this study, a case of intracranial hemorrhage in a fetus with hydrops fetalis due to Rh alloimmunization ... Sonographic Demonstration of Intracranial Hemorrhage in a Fetus with Hydrops Fetalis due to Rh Alloimmunization after ... Sonographic Demonstration of Intracranial Hemorrhage in a Fetus with Hydrops Fetalis due to Rh Alloimmunization after ...
Archer on cephalopelvic disproportion hydrops fetalis: to fetal lobulation of the kidneys? That is a normal anatomic variant, ... Fetal Hydrops (Definition) Fetal hydrops ( erythroblastosis fetalis) - excess/ abnormal amount of fluid in 2 or more fetal ... Pregnancy 15 week, ultrasound report.,.. Turner syndrome with cystic hygroma and hydrops fetalis....., your advise required? ... is termed hydrops fetalis. It could be immune or non-immune. It has to be managed by a high risk specialist who can explain ...
High-Risk Newborns - Hydrops Fetalis. What is hydrops fetalis?. Hydrops fetalis is a severe, life-threatening problem of severe ... Treatment for hydrops fetalis. Specific treatment for hydrops fetalis will be determined by your babys doctor based on:. *Your ... What are the symptoms of hydrops fetalis?. The following are the most common symptoms of hydrops fetalis. However, each baby ... The incidence of hydrops can vary between populations.. Why is hydrops fetalis a concern?. The severe edema that occurs with ...
In 51 cases with non-immunologic hydrops fetalis (NIHF), perinatal management was performed based on our protocol. Twenty-two ... Intrauterine treatment on non-immune hydrops fetalis. Maeda H, Koyanagi T, Nakano H. ...
... once the most common conditions associated with fetal ascites or hydrops have been ruled out, are important. This paper ... LSD should be considered in transient hydrops. Enzymatic studies in chorionic villous sample or amniotic cultured cells, ... Patients and methods: We report four cases with transient hydrops fetalis resulting from LSD and performed a literature review ... Lysosomal storage disorder in non-immunological hydrops fetalis (NIHF): more common than assumed? Report of four cases with ...
Rh factor react with fetus and cause hydrops fetalis,/b,? Is it concerned with their permeability through the placenta? ... Home » Frequently asked Questions on Health » Why does the Rh factor react with the fetus and cause hydrops fetalis? ... Why does the Rh factor react with the fetus and cause hydrops fetalis?. ... The typical diagnostic findings are jaundice, pallor, hepatosplenomegaly, and hydrops fetalis in severe cases. ...
We reported the first patient with early onset cobalamin C disease (cblC) who presented with non-immune hydrops fetalis, who ... Noncompaction of the ventricular myocardium and hydrops fetalis in cobalamin C disease. Response to letter "Disappearance of ...
Intraperitoneal administration of antiarrhythmic drugs to the fetus in fetal tachyarrhythmias with severe hydrops fetalis ...
hydrops fetalis associated with ABO isoimmunization (O36.1-). *hydrops fetalis associated with rhesus isoimmunization (O36.0-) ... Maternal care for hydrops fetalis. 2016 2017 2018 Non-Billable/Non-Specific Code Applicable To*Maternal care for hydrops ... Maternal care for hydrops fetalis, unspecified trimester, fetus 3. 2016 2017 2018 Billable/Specific Code Maternity Dx (12-55 ... Short description: Maternal care for hydrops fetalis, unsp trimester, fetus 3. *The 2018 edition of ICD-10-CM O36.20X3 became ...
If you are looking for information on Hydrops fetalis, reading this post may help you in understanding the causes, symptoms, ... There are two types of hydrops fetalis - Immune Hydrops Fetalis and Non-Immune Hydrops Fetalis. As the names suggest, these are ... What Is Hydrops Fetalis? Hydrops Fetalis is characterised by abnormal amounts of fluids that accumulate in two or more body ... Treatment of Hydrops Fetalis The treatment depends on the cause of hydrops fetalis, and if no evident cause is established, the ...
... hydrops fetalis explanation free. What is hydrops fetalis? Meaning of hydrops fetalis medical term. What does hydrops fetalis ... Looking for online definition of hydrops fetalis in the Medical Dictionary? ... fetal hydrops (hydrops feta´lis) gross edema of the entire body of the newborn infant, in erythroblastosis fetalis. ... fe·tal hy·drops. , hydrops fetalis. abnormal accumulation of serous fluid in the fetal tissues, as in erythroblastosis fetalis. ...
Immune Hydrops Fetalis, also known as immune fetal hydrops, is related to hydrops fetalis, nonimmune and hydrops fetalis. An ... MalaCards integrated aliases for Immune Hydrops Fetalis:. Name: Immune Hydrops Fetalis 60 74 ... MalaCards organs/tissues related to Immune Hydrops Fetalis:. 42 Bone, Lung, Testes, Pituitary, Bone Marrow ... Articles related to Immune Hydrops Fetalis:. (show top 50) (show all 115) #. Title. Authors. Year. ...
Cukierski, M. A. ; Tarantal, A. F. ; Hendrickx, A. G. / A case of nonimmune hydrops fetalis with a rare cardiac anomaly in a ... A case of nonimmune hydrops fetalis with a rare cardiac anomaly in a rhesus monkey. / Cukierski, M. A.; Tarantal, A. F.; ... Cukierski, M. A., Tarantal, A. F., & Hendrickx, A. G. (1986). A case of nonimmune hydrops fetalis with a rare cardiac anomaly ... A case of nonimmune hydrops fetalis with a rare cardiac anomaly in a rhesus monkey. Journal of Medical Primatology. 1986;15(3): ...
... - Klassifikation nach ICD 10 P56 Hydrops fetalis durch hämolytische Krankheit P83.2 Hydrops fetalis, nicht ... Endolymphatic hydrops is Ménière s disease. ** Hydrops fetalis is edema in a fetus.Zoology* Hydrops , a monotypic snake genus ... hydrops fetalis immune - hydrops fetalis caused by maternal sensitization to a fetal blood group antigen; see erythroblastosis ... Hydrops fetalis - DiseaseDisorder infobox Name = Hydrops fetalis not due to haemolytic disease/isoimmunization ICD10 = ICD10,P, ...
Fetal hydrops can be immune or nonimmune. Ninety percent are nonimmune (not the result of red cell alloimmunization). ... Hydrops fetalis is the presence of excessive fluid in two or more fetal compartments including skin edema, pleural effusion, ... Hydrops fetalis is the presence of excessive fluid in two or more fetal compartments including skin edema, pleural effusion, ... Nonimmune hydrops fetalis (NHF) can present as uterine size greater than dates due to polyhydramnios, decreased fetal movement ...
hydrops fetalis NOS (. ICD-10-CM Diagnosis Code P83.2. Hydrops fetalis not due to hemolytic disease. 2016 2017 2018 2019 2020 ... P56.9 Hydrops fetalis due to other and unspecified hemolytic disease P56.90 Hydrops fetalis due to unspecified hemolytic ... Hydrops fetalis due to hemolytic disease. 2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code *P56 should not be used for ... P56 Hydrops fetalis due to hemolytic disease P56.0 Hydrops fetalis due to isoimmunization ...
Hydrops fetalis Hydrops fetalis is a serious condition of the fetus or newborn. It is a condition where abnormal amounts of ...
  • Nonimmune hydrops fetalis is more common. (medlineplus.gov)
  • Immune and nonimmune hydrops fetalis. (medlineplus.gov)
  • Congenital Hypothyroidism and Nonimmune Hydrops Fetalis: Associated? (aappublications.org)
  • Here, we have identified an autosomal dominant, inherited form of lymphatic-related (nonimmune) hydrops fetalis (LRHF). (jci.org)
  • Independent exome sequencing projects on 2 families with a history of in utero and neonatal deaths associated with nonimmune hydrops fetalis uncovered 2 heterozygous missense variants in the gene encoding Eph receptor B4 ( EPHB4 ). (jci.org)
  • Brinson, R.A., and Goldsmith, J.P.: Nonimmune hydrops fetalis associated with intrauterine intussusception. (springer.com)
  • Nonimmune hydrops fetalis is the final common pathway of many conditions that ultimately result in fetal anasarca. (aappublications.org)
  • To our knowledge, this is the first report of midaortic syndrome as an etiology for nonimmune hydrops fetalis. (aappublications.org)
  • Frequency of parvovirus B19 infection in nonimmune hydrops fetalis and utility of three diagnostic methods. (thefreedictionary.com)
  • A case of nonimmune hydrops fetalis with a rare cardiac anomaly in a rhesus monkey. (elsevier.com)
  • A case of nonimmune hydrops fetalis in a rhesus monkey was identified by ultrasound. (elsevier.com)
  • Nonimmune hydrops fetalis (NHF) can present as uterine size greater than dates due to polyhydramnios, decreased fetal movement, fetal compromise on fetal testing, and ultrasound findings. (exxcellence.org)
  • Society for maternal-fetal medicine (SMFM) clinical guideline #7: nonimmune hydrops fetalis. (exxcellence.org)
  • Nonimmune hydrops - There is no one process to explain this type of hydrops. (medicalfoxx.com)
  • Nonimmune hydrops fetalis (NHF) is an abnormal accumulation of fluid - especially serous - in visceral cavities and soft tissues. (nel.edu)
  • OBJECTIVES: To present our experience of using OK-432 in treating fetal cystic hygroma and chylothorax complicated with nonimmune hydrops fetalis. (ntu.edu.tw)
  • Erythroblastosis fetalis, also known as Rh disease, is a hemolytic disease of newborns. (wikipedia.org)
  • In many case of hydrops fetalis, the etiology is different from that of erythroblastosis fetalis (EF). (springer.com)
  • fetal hydrops ( hydrops feta´lis ) gross edema of the entire body of the newborn infant, in erythroblastosis fetalis. (thefreedictionary.com)
  • massive edema in the fetus or newborn, usually in association with severe erythroblastosis fetalis. (thefreedictionary.com)
  • What is Erythroblastosis Fetalis? (medindia.net)
  • Erythroblastosis fetalis, also called hemolytic disease of the newborn (HDN), usually occurs in the fetus, but can also occur in the neonate (erythroblastosis neonatorum). (medindia.net)
  • What are the Causes of Erythroblastosis Fetalis? (medindia.net)
  • Erythroblastosis fetalis can be caused due to incompatibility of either of two major blood types. (medindia.net)
  • The fetal bone marrow reacts to the hemolytic anemia by releasing immature RBCs called erythroblasts into the fetal peripheral circulation, causing erythroblastosis fetalis. (medindia.net)
  • There are other minor blood group antigens that the fetus may carry, which can increase the risk of erythroblastosis fetalis. (medindia.net)
  • What are the Symptoms and Signs of Erythroblastosis Fetalis? (medindia.net)
  • The clinical features of erythroblastosis fetalis result from destruction of fetal RBCs by maternal antibodies against them. (medindia.net)
  • How do you Diagnose Erythroblastosis Fetalis? (medindia.net)
  • It's also called erythroblastosis fetalis. (ahealthyme.com)
  • This is called erythroblastosis fetalis during pregnancy. (ahealthyme.com)
  • Hydrops foetalis or hydrops fetalis is a condition in the fetus characterized by an accumulation of fluid, or edema, in at least two fetal compartments. (wikipedia.org)
  • Hydrops fetalis is a serious condition of the fetus or newborn. (medlineplus.gov)
  • Hydrops fetalis (fetal hydrops) is a serious condition in which a fetus becomes extremely swollen from buildup of fluids in the body tissues. (healthlinkbc.ca)
  • Even with treatment, fetal hydrops can cause death of the fetus. (healthlinkbc.ca)
  • The majority of hydrops fetalis cases are non-immune conditions that present with generalized edema of the fetus. (uniprot.org)
  • The majority of hydrops fetalis cases are nonimmune conditions that present with generalized edema of the fetus, and approximately 15% of these nonimmune cases result from a lymphatic abnormality. (jci.org)
  • Often he or she is confronted with a stillborn, frequently a macerated, hydropic fetus, and is asked to provide an idea as to the mechanism that led to the fetal hydrops. (springer.com)
  • Benacerraf, B.R., and Frigoletto, F.D.: In utero treatment of a fetus with diaphragmatic hernia complicated by hydrops. (springer.com)
  • We report a late onset of a hydrops fetalis seen in a fetus at 34 completed weeks of gestation. (biomedsearch.com)
  • We present a case of midaortic syndrome, also known as abdominal coarctation syndrome, in a fetus with hydrops and a severe cardiomyopathy. (aappublications.org)
  • Hydrops fetalis is a severe, life-threatening problem of severe edema (swelling) in the fetus and newborn. (nyhq.org)
  • Why does the Rh factor react with the fetus and cause hydrops fetalis? (ndtv.com)
  • Why do other blood group antigens like A, O, AB and B from the mother side not react with the fetus and why does only the Rh factor react with fetus and cause hydrops fetalis ? (ndtv.com)
  • Rhesus (Rh) hemolytic disease of the newborn represents a broad spectrum of symptoms in the fetus and newborn, ranging from mild to severe hemolytic anemia and hydrops fetalis. (acibadem.edu.tr)
  • We report the rare occurrence of an enteric cyst that presented in a fetus as a cystic intrathoracic lesion with associated hydrothorax and eventually fetal hydrops. (elsevier.com)
  • A fetus can develop congenital anemia ("Hydrops Fetalis") in the uterus. (thebody.com)
  • Fetalis means fetus. (ahealthyme.com)
  • Hydrops fetalis , which is characterized by extreme edema (abnormal accumulation of serous fluid) and congestive heart failure, is the most severe form of the disease in newborns. (britannica.com)
  • Twin-twin transfusion syndrome (TTTS) in pregnancies in which twins share a single placenta (hydrops affects the recipient twin) Twin anemia-polycythemia sequence (TAPS) Twin reversed arterial perfusion sequence (TRAPS) Maternal hyperthyroidism Fetal cardiac defects and skeletal defects Noonan syndrome Mirror syndrome, in which fetal and placental hydrops develops in association with maternal preeclampsia, edema and hypertension Down syndrome Hydrops fetalis can be diagnosed and monitored by ultrasound scans. (wikipedia.org)
  • The severe edema that occurs with hydrops can overtake the baby's organ systems. (nyhq.org)
  • Hydrops fetalis is the presence of excessive fluid in two or more fetal compartments including skin edema, pleural effusion, pericardial effusion, ascites, and polyhydramnios. (exxcellence.org)
  • Hydrops fetalis which is also known as hydrops, is a life-threatening condition in which an abnormal fluid is accumulated in two or more fetal compartments such as skin edema, pleural effusion, and pericardial effusion. (medicalfoxx.com)
  • En fetalis de los hydrops, el edema severo y peligroso para la vida (hinchazón) se convierte mientras que el líquido aumenta y rodea los pulmones, el abdomen y el corazón del feto. (news-medical.net)
  • In 51 cases with non-immunologic hydrops fetalis (NIHF), perinatal management was performed based on our protocol. (pptaglobal.org)
  • Lysosomal storage disorder in non-immunological hydrops fetalis (NIHF): more common than assumed? (nih.gov)
  • Lysosomal storage disorders (LSD) are a rare cause of non immunological hydrops fetalis (NIHF) and congenital ascites. (nih.gov)
  • We report four cases with transient hydrops fetalis resulting from LSD and performed a literature review on LSD with NIHF and congenital ascites in combination. (nih.gov)
  • The objective of our study was to evaluate the usefulness of immunohistochemical (IHC) staining techniques in the etiological diagnosis of non-immune hydrops fetalis (NIHF). (elsevier.com)
  • Human parvovirus B19 (B19) infection during pregnancy is associated with the adverse foetal outcome known as non-immune hydrops fetalis (NIHF). (microbiologyresearch.org)
  • N2 - Aim: The study was designed to document the incidence of non-immune hydrops fetalis (NIHF) at birth and characterise associated outcomes and obstetric complications. (lu.se)
  • Ultrasound examination confirmed fetal hydrops with hydrothorax and ascitis, fetal anemia (middle cerebral artery peak systolic velocity: 74.3 cm/sg with an estimated haemoglobin of 7.14 g/dl), polyhydramnios (maximum pocket 14), estimated fetal weight of 2460 g and mild cardiomegaly (cardiac area more than 1/3 of thoracic area) with hyperdinamic heart circulation. (biomedcentral.com)
  • The abnormal collection of fluid in more than one area of the fetal body, ascites or effusions, is termed hydrops fetalis. (healthtap.com)
  • Enzymatic studies in chorionic villous sample or amniotic cultured cells, once the most common conditions associated with fetal ascites or hydrops have been ruled out, are important. (nih.gov)
  • Even after extensive evaluation, the etiology of a small percentage of cases of hydrops remains unknown. (aappublications.org)
  • Immune hydrops fetalis is most often a complication of a severe form of Rh incompatibility , which can be prevented. (medlineplus.gov)
  • The number of babies who develop immune hydrops fetalis has dropped due to a medicine called RhoGAM. (medlineplus.gov)
  • There are other, much rarer, blood group incompatibilities that can also cause immune hydrops fetalis, but RhoGAM does not help with these. (medlineplus.gov)
  • For immune hydrops, direct transfusion of red blood cells that match the infant's blood type. (medlineplus.gov)
  • Non-immune hydrops can also be unrelated to anemia, for example if a fetal tumor or congenital cystic adenomatoid malformation increases the demand for blood flow. (wikipedia.org)
  • A form of non-immune hydrops fetalis, a condition characterized by fluid accumulation in at least 2 fetal compartments, including abdominal cavities, pleura, and pericardium, or in body tissue. (uniprot.org)
  • Immune hydrops may develop because of Rh disease in the mother. (nyhq.org)
  • Non-immune hydrops includes all other diseases or complications that may interfere with the baby's ability to manage fluid. (nyhq.org)
  • There is no one mechanism to explain non-immune hydrops. (nyhq.org)
  • Immune hydrops is not as common as it used to be since the widespread use of Rh immunoglobulin treatment for Rh negative women. (nyhq.org)
  • Non-immune hydrops occurs rarely. (nyhq.org)
  • Intrauterine treatment on non-immune hydrops fetalis. (pptaglobal.org)
  • We reported the first patient with early onset cobalamin C disease ( cbl C) who presented with non-immune hydrops fetalis, who also had left ventricular noncompaction (LVNC) and heart failure in the neonatal period. (springer.com)
  • There are two types of hydrops fetalis - Immune Hydrops Fetalis and Non-Immune Hydrops Fetalis. (firstcry.com)
  • Extreme cases of Rh-incompatibility can cause immune hydrops. (firstcry.com)
  • Non-immune hydrops fetalis is more common and occurs when some kind of disease or ailment hampers with the body's ability to regulate fluids. (firstcry.com)
  • Some of the health conditions that can lead to non-immune hydrops fetalis include chromosomal abnormalities , congenital infections, severe anaemia , etc. (firstcry.com)
  • If the baby has immune hydrops, she could receive a red blood transfusion. (firstcry.com)
  • Immune Hydrops Fetalis, also known as immune fetal hydrops , is related to hydrops fetalis, nonimmune and hydrops fetalis . (malacards.org)
  • An important gene associated with Immune Hydrops Fetalis is GUSB (Glucuronidase Beta), and among its related pathways/superpathways are Lysosome and Binding and Uptake of Ligands by Scavenger Receptors . (malacards.org)
  • Immune hydrops - They might develop because of Rh disease that is present in the mother. (medicalfoxx.com)
  • Cholestasis is a common problem in infants with immune hydrops fetalis (IHF). (acibadem.edu.tr)
  • In conclusion, specific IHC staining techniques aimed at detecting lymphatic dysplasia are needed and should be mandatory in autopsies of fetuses with non-immune hydrops fetalis. (elsevier.com)
  • Start Forskningsoutput Non-immune hydrops fetalis was rare in Sweden during 1997-20. (lu.se)
  • Non-immune hydrops fetalis as a diagnostic and survival problems: what do we tell the parents? (degruyter.com)
  • Congenital disorders of glycosylation Parvovirus B19 (fifth disease) infection of the pregnant woman (Most Common cause) Cytomegalovirus in mother Congenital pulmonary airway malformation (formerly called congenital cystic adenomatoid malformation) Maternal syphilis and maternal diabetes mellitus Alpha-thalassemia can also cause hydrops fetalis when all four of the genetic loci for α globin are deleted or affected by mutation. (wikipedia.org)
  • Timely referral to a maternal-fetal medicine specialist allows for detailed and comprehensive ultrasonographic examination and the early identification of any treatable causes of fetal hydrops. (medscape.com)
  • If fetal hydrops is suspected, syphilis serology is mandatory, with repeat serial testing and, very importantly, with dilution of maternal serum. (medscape.com)
  • The prozone effect has been demonstrated repeatedly with fetal hydrops due to syphilis, thus dilution of maternal serum to avoid false-negative results is required. (medscape.com)
  • Maternal serum screening tests (multiple-marker, triple-screen, triple-marker), commonly used if fetal anomaly is suspected, are of uncertain value with fetal hydrops. (medscape.com)
  • Bernstein, I.M., and Capeless, E.L.: Elevated maternal serum alpha-fetoprotein and hydrops fetalis in association with fetal parvovirus B-19 infection. (springer.com)
  • We report a case of giant chorioangioma with fetal hydrops, additionally complicated by severe anemia, mild cardiomegaly with hyperdinamic heart circulation and maternal mirror syndrome. (biomedcentral.com)
  • A 34-year-old woman, gravida 1, was referred to our Department at 29 weeks´ gestation because of placental chorioangioma, severe hydrops fetalis, suspected fetal anemia and maternal mirror syndrome (Ballantine's syndrome), previously not detected. (biomedcentral.com)
  • After adjustment for maternal gravidity, parity, and history of affected offspring, the odds ratio for development of hydrops by male fetuses was 13.1 (95% CI 2.69-63.6, p = 0.001). (nih.gov)
  • Hydrops Fetalis is a severe and life-threatening condition that can affect fetuses or newborn babies. (firstcry.com)
  • Details are presented of analyses of hemoglobins in blood samples from four newborn babies with hydrops fetal is using reversed phase and anion exchange high performance liquid chromatographic methodology. (elsevier.com)
  • A newborn with hydrops fetalis may have severe swelling of their entire body. (ahealthyme.com)
  • This test or hydrops fetalis ultrasound will help the doctor is establishing how the blood is flowing in different parts of the baby's baby. (firstcry.com)
  • Antenatal ultrasound scanning enables early recognition of hydrops fetalis. (enacademic.com)
  • These findings in the first trimester usually carry a poor outlook for survival of the baby but there have been many reports of resolution of both cystic hygroma and hydrops as pregnancy progresses. (healthtap.com)
  • During pregnancy, hydrops may be treatable only in certain situations. (nyhq.org)
  • therefore, if this condition is detected in babies, correct treatment measures must be taken at the earliest to increase the chances of successful pregnancy after hydrops. (firstcry.com)
  • But with each subsequent pregnancy, the risk for hydrops increases. (drgreene.com)
  • citation needed] Hydrops fetalis usually stems from fetal anemia, when the heart needs to pump a much greater volume of blood to deliver the same amount of oxygen. (wikipedia.org)
  • The non-immune form of hydrops fetalis has many causes including: Iron deficiency anemia Paroxysmal supraventricular tachycardia resulting in heart failure Deficiency of the enzyme beta-glucuronidase. (wikipedia.org)
  • Hydrops can develop as the baby's organs are unable to compensate for the anemia. (nyhq.org)
  • Hydrops may resolve in some cases when the anemia is corrected. (exxcellence.org)
  • Hydrops fetalis can form as the organs of the baby are not able to make up for the anemia. (medicalfoxx.com)
  • Severe G6PD deficiency can cause severe anemia and increased bilirubin and can cause hydrops fetalis. (healthtap.com)
  • In one study, positive screening tests (any of the three used) with only a 60% sensitivity in 19 cases of Turner syndrome distinguished some fetuses with cystic hygroma and/or hydrops from those without. (medscape.com)
  • The deficiency has presented as hydrops fetalis and HELLP syndrome in fetuses. (wikipedia.org)
  • We conclude, that in every case of hydrops fetalis the venous system should be evaluated by ultrasonography prenatally and/or immediately postnatally. (biomedsearch.com)
  • The rate of survival often depends on the cause and treatment of hydrops fetalis. (medicalfoxx.com)
  • By comparison, hydrops allantois or hydrops amnion is an accumulation of excessive fluid in the allantoic or amniotic space, respectively. (wikipedia.org)
  • Hydrops fetalis describes fluid accumulation in at least 2 fetal compartments, including abdominal cavities, pleura, and pericardium, or in body tissue. (jci.org)
  • Hydrops develops when too much fluid leaves the bloodstream and goes into the tissues. (nyhq.org)
  • Excess amounts of amniotic fluid or abnormally large or thick placenta (placental hydrops). (firstcry.com)
  • hydrops fetalis - the accumulation of fluid in fetal tissues or body cavities. (enacademic.com)
  • This report describes a case of fetal mediastinal teratoma complicated by hydrops fetalis managed successfully by aspiration of the tumor cyst fluid. (elsevier.com)
  • The hydrops resolved after fetal aspiration of the tumor cyst fluid. (elsevier.com)
  • Hydrops fetalis forms when an excessive amount of fluid departs from the bloodstream and goes directly into the tissues. (medicalfoxx.com)
  • The type of hydrops fetalis will depend on the cause of the abnormal fluid. (medicalfoxx.com)
  • Turner syndrome with cystic hygroma and hydrops fetalis. (healthtap.com)
  • The patient presented with a large cystic mass in the thoracic cavity complicated by hydrops fetalis. (elsevier.com)
  • Detection of [alpha]-thalassemia in [beta]-thalassemia carriers and prevention of Hb Bart's hydrops fetalis through prenatal screening. (thefreedictionary.com)
  • Hb Bart's hydrops fetalis is the most severe form of alpha-thalassemia (see this term) and is almost always lethal. (mendelian.co)
  • Hb Bart's Hydrops Fetalis Is also known as alpha-thalassemia major, alpha-thalassemia hydrops fetalis, homozygous alpha0-thalassemia, hemoglobin bart's hydrops fetalis. (mendelian.co)
  • Treatment of hydrops depends on the cause. (nyhq.org)
  • The treatment depends on the cause of hydrops fetalis, and if no evident cause is established, the doctor may suggest measures to ease the symptoms. (firstcry.com)
  • There are two types of hydrops fetalis, immune and nonimmune. (medlineplus.gov)
  • What are the symptoms of hydrops fetalis? (nyhq.org)
  • The following are the most common symptoms of hydrops fetalis. (nyhq.org)
  • The symptoms of hydrops fetalis may resemble other conditions or medical problems. (nyhq.org)
  • Symptoms vary on the severity of hydrops fetalis and may differ on each baby. (medicalfoxx.com)
  • This is a type of hydrops which occurs when there is an RH-incompatibility between the fetal and mother's blood. (firstcry.com)
  • Fetal mediastinal teratomas are rare tumors that cause hydrops fetalis or fetal demise in the prenatal period and respiratory distress in the neonatal period. (elsevier.com)
  • Mediastinal shift and hydrops fetalis are indications for fetal intervention. (nature.com)
  • P83.2 is a billable ICD code used to specify a diagnosis of hydrops fetalis not due to hemolytic disease. (icd.codes)
  • Hydrops fetalis (HF) is a diagnosis with significant morbidity and mortality. (actamedicaphilippina.com.ph)
  • Radiofrequency catheter ablation in a haemodynamically compromised premature neonate with hydrops fetalis. (biomedsearch.com)
  • Diseases associated with EPHB4 include Hydrops Fetalis, Nonimmune, And/Or Atrial Septal Defect and Hydrops Fetalis . (genecards.org)
  • Nonimmune - This is the more typical type of hydrops fetalis. (medicalfoxx.com)
  • Fetal metabolic storage diseases cause hydrops due to congestion caused by accumulation of metabolites in the liver and other abdominal viscera. (exxcellence.org)
  • If left untreated, hydrops can stress the baby's vital organs and lead to life-threatening complications. (firstcry.com)
  • Hydrops fetalis can develop for a variety of reasons, such as from problems related to Rh sensitization or chromosomal abnormalities. (healthlinkbc.ca)
  • Our outcome raises the issue whether additional intrauterine clinical intervention, as intersticial laser, should have been performed to stop further deterioration of the fetal condition when progressive severe hydrops develops. (biomedcentral.com)
  • Intrauterine parvovirus infection associated with hydrops fetalis. (microbiologyresearch.org)
  • Hydrops fetalis often results in death of the infant shortly before or after delivery. (medlineplus.gov)
  • however, DS-TAM neonates with hydrops fetalis (HF) show poor clinical outcomes. (elsevier.com)
  • abstract = "We report the successful management of a case of hemolytic disease and hydrops fetalis secondary to anti Rh 17 antibodies in a woman with the rare D - - phenotype. (elsevier.com)