Hydrops Fetalis
Endolymphatic Hydrops
Fetal Diseases
Parvovirus B19, Human
Blood Transfusion, Intrauterine
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.
alpha-Thalassemia
Rh Isoimmunization
Hemoglobins, Abnormal
Erythema Infectiosum
Cystic Adenomatoid Malformation of Lung, Congenital
Prenatal Diagnosis
Polyhydramnios
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.
Ultrasonography, Prenatal
Pregnancy
alpha-Globins
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.
Hemoglobin H
Edema
Mucopolysaccharidosis VII
Phosphotransferases (Phosphomutases)
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.
Thalassemia
Hypoalbuminemia
Gestational Age
Amniocentesis
Meniere Disease
Fatal Outcome
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)A case of nonimmune hydrops fetalis with a rare cardiac anomaly in a rhesus monkey.<...
Midaortic Syndrome in the Fetus and Premature Newborn: A New Etiology of Nonimmune Hydrops Fetalis and Reversible Fetal...
Immunohistochemistry in non-immune hydrops fetalis: A single center experience in 79 fetuses<...
Antenatal Treatment of Chylothorax and Cystic Hygroma with Ok-432 in Nonimmune Hydrops Fetalis | NTU Scholars
Nonimmune hydrops fetalis due to congenital syphilis associated with negative intrapartum maternal serology screening -...
Hydrops fetalis, non-immune, and/or atrial septal defect
Etiology of Hydrops Fetalis at the Philippine General Hospital: A Retrospective Study | Acta Medica Philippina : The National...
Exchange transfusion and cytarabine for transient abnormal myelopoiesis in hydrops fetalis<...
Management of non-immune hydrops: 8 Years experience<...
Why does the Rh factor react with the fetus and cause hydrops fetalis?
Hydrops fetalis | Nicklaus Childrens Hospital
HKU Scholars Hub: Variable levels of mosaicism for trisomy 21 in a non-immune hydropic infant with chylothorax
Science Update: DNA sequencing technique helpful for identifying genetic causes of fetal fluid buildup, NIH-funded study...
ICD-10-CM Code P56.90 - Hydrops fetalis due to unspecified hemolytic disease
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Effect of anaemia on fetal acid-base status. - Semantic Scholar
Carnitine deficiency with cardiomyopathy presenting as neonatal hydrops: Successful response to carnitine therapy | SpringerLink
Congenital anomalies and termination of pregnancy in Iran
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Definitions of erythroblastosis fetalis - OneLook Dictionary Search
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Enrichment and Characterization of the Tumor Immune and Non-immune Microenvironments in Established Subcutaneous Murine Tumors ...
Cephalopelvic disproportion hydrops fetalis - New Doctor Insights
SCS eNews: Interstitial deletion of chromosome 1 (1p21.1p12) in an infant with congenital diaphragmatic hernia, hydrops fetalis...
Erythroblastosis fetalis - definition of erythroblastosis fetalis by The Free Dictionary
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Erythroblastosis fetalis. Causes, symptoms, treatment Erythroblastosis fetalis
Diagnosis and incidence of fetal parvovirus infection in an autopsy series: I. Histology<...
Corneal hydrops - Wikipedia
Diagnosis of fetal urinary tract malformations: prenatal management and postnatal outcome.
Immune fetal hydrops definition | Drugs.com
Acute corneal hydrops in keratoconus: a national prospective study of incidence and management.
Gene deletions in alpha thalassemia prove that the 5 zeta locus is functional. - Radcliffe Department of Medicine
Alpha zero-thalassemia due to recombination between the alpha 1-globin gene and an AluI repeat - Radcliffe Department of...
Uncomplicated Fetal Tachycardia in Labour: Dilemmas and Uncertainties - Irish Medical Journal
High rate of severe fetal outcomes associated with maternal parvovirus B19 infection in pregnancy<...
Fetal tachycardia : intrauterine and postnatal course
Erythroblastosis Fetalis - Causes, Symptoms, Diagnosis, Treatment & Prevention
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Hydrops Management
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Hydrops fetalis
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 ... Erythroblastosis fetalis, also known as Rh disease, is the only immune cause of hydrops fetalis. 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 ...
Pulmonary hypoplasia
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 ...
Hemolytic disease of the newborn (anti-Kell)
Hydrops fetalis can also occur early. The finding of anti-Kell antibodies in an antenatal screening blood test (indirect Coombs ... as well as fetal signs of anemia or hydrops. Blood is generally drawn from the father to help determine fetal antigen status. ...
Joseph Demarco
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 ...
Rh factor testing
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-ectopic calcification-moth-eaten skeletal dysplasia
The second defining feature of hydrops-ectopic calcification-moth-eaten skeletal dysplasia is hydrops fetalis. A condition ... "Hydrops Fetalis: Causes, Outlook, Treatment and More". Healthline. Retrieved June 23, 2021. v t e (CS1: long volume value, ... Ectopic calcification Hydrops Trajkovski Z, Vrcakovski M, Saveski J, Gucev ZS (September 2002). "Greenberg dysplasia (hydrops- ... Hydrops-ectopic calcification-moth-eaten skeletal dysplasia causes the bones in a fetus to develop abnormally. This leads to a ...
Transient myeloproliferative disease
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 ...
Blood type
Sometimes this is lethal for the fetus; in these cases it is called hydrops fetalis. If a pregnant woman is known to have anti- ...
Generalized arterial calcification of infancy
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 ...
David Hager
Nonimmune hydrops fetalis associated with maternal infection with syphilis. Am J Obstet Gynecol 167:56, 1992. Hager WD, Rapp RP ...
Njølstad syndrome
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 ...
Tracheal agenesis
... 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 ( ...
Teratoma
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
"KLF1-null neonates display hydrops fetalis and a deranged erythroid transcriptome". Blood. 125 (15): 2405-17. doi:10.1182/blood ...
Alpha-thalassemia
More specifically, HbH disease is seen in Southeast Asia and the Middle East, while Hb Bart hydrops fetalis is acknowledged in ... Songdej D, Babbs C, Higgs DR (March 2017). "An international registry of survivors with Hb Bart's hydrops fetalis syndrome". ...
Transfusion-dependent anemia
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 ... Hemoglobin Barts hydrops fetalis is the most severe form of alpha-thalassemia, and individuals with this disease have severe ...
Hemoglobin Barts
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". ...
HADHB
The deficiency has presented as hydrops fetalis and HELLP syndrome in fetuses. A compound heterozygous mutation of the HADHB ...
Transaldolase 1
... 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. ...
Fifth disease
The review showed that those born with parvovirus B19 that caused hydrops fetalis did have an association with higher mortality ... In some cases, fetuses would develop hydrops fetalis due to congenital parvovirus B19. This condition was studied as a ... Vertical transmission from maternal infection may also occur, which can lead to hydrops fetalis due to the infection's ... infection in the first trimester has been linked to hydrops fetalis, causing spontaneous miscarriage. In people with sickle- ...
Beta-glucuronidase
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 ...
Zika fever
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. ...
Farm Sanctuary
... claims increased rates of hydrops fetalis, Large Offspring Syndrome, and other systemic abnormalities. Farm ...
Congenital heart block
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 ...
David Todd (haematologist)
... hydrops fetalis)". Nature. 251 (5474): 392-393. Bibcode:1974Natur.251..392T. doi:10.1038/251392a0. PMID 4424635. S2CID 4154498 ...
Yuet Wai Kan
... hydrops fetalis)". Nature. 251 (5474): 392-393. Bibcode:1974Natur.251..392T. doi:10.1038/251392a0. PMID 4424635. S2CID 4154498 ...
Congenital pulmonary airway malformation
... 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 × ...
Adrenomedullin
The adrenomedullin knockout is an embryonic lethal phenotype and dies mid gestation from a condition known as hydrops fetalis. ...
Edema
Hydrops fetalis is a condition in a baby characterized by an accumulation of fluid in at least two body compartments. The ...
Hypochondrogenesis
The abdomen is enlarged, and excess fluid may build up in the body before birth (a condition called hydrops fetalis). As a ... hydrops fetalis, pulmonary hypoplasia, and a cleft palate. Hypochondrogenesis is one of the most severe conditions in a ...
Simpson-Golabi-Behmel syndrome
... hydrops fetalis, increased nuchal translucency, craniofacial abnormalities, visceromegaly, renal abnormalities, congenital ...
Glucose-6-phosphate isomerase
... and a severe enzyme deficiency can be associated with hydrops fetalis, immediate neonatal death and neurological impairment. ...
Parvovirus B19
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 and Gynecology. 109 ...
Hereditary spherocytosis
... in-utero hydrops fetalis), because HS is caused by genetic mutations in a multitude of structural membrane proteins and ...
List of fetal abnormalities
... femoral hypoplasia Gastrointestinal atresia Gastroschisis Holoprosencephaly Hydranencephaly Hydronephrosis Hydrops fetalis ...
Achondrogenesis type 2
... and affected infants often have a condition called hydrops fetalis in which excess fluid builds up in the body before birth. ...
Parvoviridae
... hydrops fetalis in pregnant women, and arthropathy. Human bocavirus 1 is a common cause of acute respiratory tract infection, ...
Hemolytic disease of the newborn
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). " ... "Erythroblastosis Fetalis", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 30020664, retrieved 2022-03-08 " ...
Sly syndrome
The most severe cases of Sly syndrome can result in hydrops fetalis, which results in fetal death or death soon after birth. ...
List of MeSH codes (C13)
... hydrops fetalis MeSH C13.703.277.080 - fetal alcohol syndrome MeSH C13.703.277.370 - fetal growth retardation MeSH C13.703. ...
Vertically transmitted infection
... produces hydrops fetalis secondary to aplastic anemia) T - toxoplasmosis O - other (group B streptococci, Listeria, Candida, ...
List of MeSH codes (C23)
... hydrops fetalis MeSH C23.888.307.500 - eye hemorrhage MeSH C23.888.592.162 - bladder, neurogenic MeSH C23.888.592.230 - ...
List of ICD-9 codes 760-779: certain conditions originating in the perinatal period
... enterocolitis 778 Conditions involving the integument and temperature regulation of fetus and newborn 778.0 Hydrops fetalis not ...
Amniocentesis
... hydrops fetalis, and intrauterine fetal demise. RhD immune globulin (RhoGam) is administered to prevent maternal Rh ... Nassar GN, Wehbe C (2022). "Erythroblastosis Fetalis". StatPearls. Treasure Island (FL): StatPearls Publishing. PMID 30020664. ...
List of MeSH codes (C20)
... hydrops fetalis MeSH C20.188.413.502 - kernicterus MeSH C20.543.206.380 - drug eruptions MeSH C20.543.206.380.350 - epidermal ...
Rh disease
... termed hydrops fetalis. The severe anemia taxes the heart to compensate by increasing output in an effort to deliver oxygen to ... Levine published his theory that the disease known as erythroblastosis fetalis was due to Rh alloimmunization in 1941 while ... LEVINE, P.; VOGEL, P.; KATZIN, E. M.; BURNHAM, L. (1941-10-17). "Pathogenesis of Erythroblastosis Fetalis: Statistical Evidence ... Vossoughi, Sarah; Spitalnik, Steven L. (July 2019). "Conquering erythroblastosis fetalis: 50 years of RhIG". Transfusion. 59 (7 ...
Mucopolysaccharidosis
In its rarest form, Sly syndrome causes children to be born with hydrops fetalis, in which extreme amounts of fluid are ...
Pyknoachondrogenesis
The findings that can be seen in patients with this condition include hydrops fetalis, palpebral edemas, low-set ears, abdomen ...
Hydrops fetalis: MedlinePlus Medical Encyclopedia
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 | Boston Children's Hospital
Hydrops fetalis is when large amounts of fluid build up in a babys tissues and organs, causing extensive swelling. Learn more ... Hydrops Fetalis , Symptoms & Causes. What are the symptoms of hydrops fetalis?. Symptoms of hydrops fetalis can occur during ... Hydrops Fetalis , Diagnosis & Treatments. How is hydrops fetalis diagnosed?. Hydrops fetalis can be diagnosed during pregnancy ... How is hydrops fetalis treated?. Treatment of hydrops fetalis depends on its cause. During pregnancy, hydrops fetalis is ...
Hydrops fetalis - Rare Pediatrician News
There are two types of hydrops fetalis: immune and nonimmune. Immune hydrops fetalis is a complication of a severe form of Rh ... Hydrops fetalis is a serious condition in which abnormal amounts of fluid build up in two or more body areas of a fetus or ... Nonimmune hydrops fetalis occurs when a disease or medical condition disrupts the bodys ability to manage fluid. There are ... PubMed is a searchable database of medical literature and lists journal articles that discuss Hydrops fetalis. Click on the ...
IMSEAR at SEARO: Hydrops fetalis: report of 3 cases.
Reported cases are hydrops fetalis diagnosed during ultrasonic evaluation of fetal condition in the Center for Nuclear Medicine ... Recent advances in prenatal ultrasound have made possible the early detection of hydrops fetalis which is helpful for proper ... To decrease the mortality rate and to improve the outcome of hydrops fetalis cases appropriate prenatal investigations and ... Hydrops fetalis: report of 3 cases. Mymensingh Medical Journal. 2003 Jul; 12(2): 138-41. ...
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List of ICD-10 Causes Used in WISQARS Fatal Reports - Fatal Injury Help Menu | WISQARS | Injury Center | CDC
Hypertension and Pregnancy: Overview, Chronic Hypertension, Differential Diagnosis
Hypertension is the most common medical problem encountered during pregnancy, complicating 2-3% of pregnancies. Hypertensive disorders during pregnancy are classified into 4 categories, as recommended by the National High Blood Pressure Education Program Working Group on High Blood Pressure in Pregnancy: Chronic hypertension Preeclampsia-ecla...
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Non-immune hydrops fetalis associated with impaired fetal movement: A case report and review
ICD-10-CM Code P56.9 - Hydrops fetalis due to other and unspecified hemolytic disease
BILLABLE P56.90 Hydrops fetalis due to unspecified hemolytic disease * BILLABLE P56.99 Hydrops fetalis due to other hemolytic ... The ICD code P56 is used to code Hydrops fetalis Hydrops fetalis is a condition in the fetus characterized by an accumulation ... Hydrops fetalis due to other and unspecified hemolytic disease NON-BILLABLE Non-Billable Code Non-Billable means the code is ... P56.9 Hydrops fetalis due to other and unspecified hemolytic disease NON-BILLABLE ...
Table 1 - Shuni Virus in Cases of Neurologic Disease in Humans, South Africa - Volume 27, Number 2-February 2021 - Emerging...
Genetic disorders and pregnancy outcomes of non-immune hydrops fetalis in a tertiary referral center. | BMC Med Genomics;16(1)...
Non-immune hydrops fetalis (NIHF) is a non-specific symptom associated with a wide range of disorders. The prognosis of NIHF ... In this study, we investigated the incidence of chromosomal abnormalities and Barts hydrops fetalis in pregnancies associated ... In addition, α-thalassemia genotyping was performed to confirm the presence of Barts hydrops fetalis. RESULTS:. Chromosomal ... In South China, Barts hydrops fetalis and chromosomal abnormalities are the most common genetic etiologies of NIHF. ...
Alpha Thalassemia (for Parents) - Willis-Knighton Health System
Transfusión intrauterina en hidrops fetal por Parvovirus B19: a propósito de un caso clínico
Alpha thalassemia: MedlinePlus Genetics
Alpha-thalassemia: Hb H disease and Hb Barts hydrops fetalis. Ann N Y Acad Sci. 2005;1054:25-32. doi: 10.1196/annals.1345.004. ... The more severe type is known as hemoglobin Bart hydrops fetalis syndrome, which is also called Hb Bart syndrome or alpha ... Hb Bart syndrome is characterized by hydrops fetalis, a condition in which excess fluid builds up in the body before birth. ...
Current Trends Risks Associated with Human Parvovirus B19 Infection
Human parvovirus infection in pregnancy and hydrops fetalis. N Engl J Med 1987;316:183-6. * Bond PR, Caul EO, Usher J, Cohen BJ ... Parvovirus as a cause of hydrops fetalis: detection by in situ DNA hybridisation. J Clin Pathol 1988;41:381-3. * Anderson MJ, ... In a survey of 50 fetuses with nonimmunologic hydrops fetalis, an uncommonly diagnosed cause of fetal death, four (8%) were ... Human parvovirus B19 and hydrops fetalis (Letter). Lancet 1988;1:535. * Franciosi RA, Tattersall P. Fetal infection with human ...
Possible Zika Virus Infection Among Pregnant Women - United States and Territories, May 2016 | MMWR
2013 ICD-9-CM Diagnosis Code 653.9 : Unspecified disproportion in pregnancy labor and delivery
Image IQ: A 12-Week Fetus
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Glucose phosphate isomerase deficiency as a cause of hydrops fetalis. N Engl J Med. 1987; 316:258-61. PubMedGoogle Scholar ... Ferreira P, Morais L, Costa R, Resende C, Dias CP, Araujo F. Hydrops fetalis associated with erythrocyte pyruvate kinase ... Hydrops fetalis associated with erythrocyte pyruvate kinase deficiency. Eur J Pediatr. 2000; 159:481-2. PubMedhttps://doi.org/ ...
Update and audit of the St George's classification algorithm of primary lymphatic anomalies: a clinical and molecular approach...
EPHB4 kinase-inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalis. J Clin Invest 2016;126:3080-8. ... Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis. Nat ... Etiology of non-immune hydrops fetalis: an update. Am J Med Genet A 2015;167A:1082-8.doi:10.1002/ajmg.a.36988 pmid:http://www. ... Prenatally, these conditions may present with pleural effusions (hydrothoraces), or as non-immune fetal hydrops (the ...
2023 ICD-10-CM Diagnosis Code P55.0: Rh isoimmunization of newborn
Sacrococcygeal teratoma in the perinatal period | Postgraduate Medical Journal
1994) Antenatal diagnosis of sacrococcygeal teratoma with hydrops fetalis. Eur J Pediatr Surg 4:125-127. ... A poor outcome is usually correlated with placentomegaly, cardiomegaly, or non-immune hydrops fetalis.19 ... hydrops fetalis, and bladder outlet obstruction.19 ,24-28 Some of these complications can be detected prenatally and treated ... If hydrops develops, close maternal-fetal observation is needed. Maternal corticosteroids are advisable to accelerate fetal ...
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Pre-made Human GBA knockout HeLa cell lysate (ab256929) | Abcam
Hydrops fetalis, in utero fetal death and neonatal distress are prominent features. When hydrops is absent, neurologic ... Non-immune hydrops fetalis is not a diagnosis in itself but a symptom, a feature of many genetic disorders, and the end-stage ... Note=Perinatal lethal Gaucher disease is associated with non-immune hydrops fetalis, a generalized edema of the fetus with ...