Anemia, Myelophthisic
Anemia, Aplastic
Anemia, Hemolytic
Fanconi Anemia
Congenital disorder affecting all bone marrow elements, resulting in ANEMIA; LEUKOPENIA; and THROMBOPENIA, and associated with cardiac, renal, and limb malformations as well as dermal pigmentary changes. Spontaneous CHROMOSOME BREAKAGE is a feature of this disease along with predisposition to LEUKEMIA. There are at least 7 complementation groups in Fanconi anemia: FANCA, FANCB, FANCC, FANCD1, FANCD2, FANCE, FANCF, FANCG, and FANCL. (from Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=227650, August 20, 2004)
Anemia, Hemolytic, Autoimmune
Anemia, Hypochromic
Anemia characterized by a decrease in the ratio of the weight of hemoglobin to the volume of the erythrocyte, i.e., the mean corpuscular hemoglobin concentration is less than normal. The individual cells contain less hemoglobin than they could have under optimal conditions. Hypochromic anemia may be caused by iron deficiency from a low iron intake, diminished iron absorption, or excessive iron loss. It can also be caused by infections or other diseases, therapeutic drugs, lead poisoning, and other conditions. (Stedman, 25th ed; from Miale, Laboratory Medicine: Hematology, 6th ed, p393)
Encyclopedias as Topic
Bone Marrow
The soft tissue filling the cavities of bones. Bone marrow exists in two types, yellow and red. Yellow marrow is found in the large cavities of large bones and consists mostly of fat cells and a few primitive blood cells. Red marrow is a hematopoietic tissue and is the site of production of erythrocytes and granular leukocytes. Bone marrow is made up of a framework of connective tissue containing branching fibers with the frame being filled with marrow cells.
Rare Diseases
Dyskeratosis Congenita
A predominantly X-linked recessive syndrome characterized by a triad of reticular skin pigmentation, nail dystrophy and leukoplakia of mucous membranes. Oral and dental abnormalities may also be present. Complications are a predisposition to malignancy and bone marrow involvement with pancytopenia. (from Int J Paediatr Dent 2000 Dec;10(4):328-34) The X-linked form is also known as Zinsser-Cole-Engman syndrome and involves the gene which encodes a highly conserved protein called dyskerin.
High number of circulating CD34+ cells in patients with myelophthisis. (1/10)
Six patients with bone marrow micrometastases from solid cancers presented with increased numbers of circulating CD34+ cells; the CD34+ cell counts were very high in some cases. By contrast, no patient with metastatic cancer without bone marrow involvement showed raised numbers of circulating hemopoietic progenitors. (+info)Premature labor and leukoerythroblastosis in a newborn with parvovirus B19 infection. (2/10)
Leukoerythroblastosis is a rarely observed disease characterized by the presence of leukocytosis, erythroid and myeloid blast cells in peripheral blood. To our knowledge, it had not been diagnosed in a premature newborn before the case we report have.A female baby weighing 1164 grams, who was born prematurely at the 29th week of gestation by Cesarean section was referred to our newborn intensive care unit due to prematurity and respiratory distress with no prenatal pathological findings. Physical examination revealed tachypnea and hepatosplenomegaly. Routine laboratory measurements showed significant leukocytosis (85,000/mm3) and anemia (Hb: 9.6 g/dL and Hct: 27.6%). The platelet count was normal. The peripheral blood smear suggested leukoerythroblastosis with the presence of nucleated erythrocytes, monocytosis, and 4% blasts. Bone marrow cytogenetic examination was normal. Parvovirus B19 Ig G and M serology were detected to be positive. The etiological factors observed in leukoerythroblastosis occurring during neonatal and early childhood period are congenital-postnatal viral infections, juvenile myelomonocytic leukemia and osteopetrosis. To our knowledge, no case of leukoerythroblastosis in such an early phase has been reported in the in literature. As a result, premature delivery and leukoerythroblastosis were thought to have developed secondary to intrauterine parvovirus B19 infection. Leukoerythroblastosis is a rarely observed disease characterized by the presence of leukocytosis, erythroid and myeloid blast cells in peripheral blood. It is reported that it can be observed following hematologic malignancies especially juvenile myelomonocytic leukemia, acute infections, hemolytic anemia, osteopetrosis, myelofibrosis, neuroblastoma and taking certain medicines. To our knowledge, it has not been diagnosed in a premature newborn before. Here we the case of a newborn who was referred to our intensive care unit due to being born prematurely at the 29th week of gestation and diagnosed with leukoerythroblastosis. (+info)Lenalidomide therapy in myelofibrosis with myeloid metaplasia. (3/10)
We present results of 2 similarly designed but separate phase 2 studies involving single-agent lenalidomide (CC-5013, Revlimid) in a total of 68 patients with symptomatic myelofibrosis with myeloid metaplasia (MMM). Protocol treatment consisted of oral lenalidomide at 10 mg/d (5 mg/d if baseline platelet count < 100 x 10(9)/L) for 3 to 4 months with a plan to continue treatment for either 3 or 24 additional months, in case of response. Overall response rates were 22% for anemia, 33% for splenomegaly, and 50% for thrombocytopenia. Response in anemia was deemed impressive in 8 patients whose hemoglobin level normalized from a baseline of either transfusion dependency or hemoglobin level lower than 100 g/L. Additional treatment effects in these patients included resolution of leukoerythroblastosis (4 patients), a decrease in medullary fibrosis and angiogenesis (2 patients), and del(5)(q13q33) cytogenetic remission accompanied by a reduction in JAK2(V617F) mutation burden (1 patient). Grade 3 or 4 adverse events included neutropenia (31%) and thrombocytopenia (19%). We conclude that lenalidomide engenders an intriguing treatment activity in a subset of patients with MMM that includes an unprecedented effect on peripheral blood and bone marrow abnormalities. (+info)Effects of weiganli on the hemopoietic function of the myelosuppressed anemic mice. (4/10)
OBJECTIVE: To study the effect of weiganli ([Chinese characters: see text]) on bone marrow hemopoiesis. METHODS: The effects of weiganli on the peripheral blood picture and the number of bone marrow nucleated cells (BMCs) were observed in myelosuppressed anemic model mice, and the effects of weiganli on the growth of colony forming unit-granulocyte macrophage (CFU-GM), colony forming unit-erythroid (CFU-E), burst forming unit-erythroid (BFU-E), colony forming unit-megkaryocyte (CFU-Meg) were investigated by in vitro cell culture technique. The hemopoietic stem cells (HSCs, c-kit+) in bone marrow were double stained with fluorescent antibody PE-C-Kit and FITC-CD45, and the HSCs (c-kit+) were counted by flow cytometer with CD45/SSC (side scatter) gating. RESULTS: Peripheral blood cell counts and the number of BMCs were significantly improved after weiganli administration; and bone marrow hemopoietic stem/progenitor cells were significantly increased. CONCLUSION: Weiganli can effectively promote the recovery of hemopoietic function in the myelosuppressed anemic mice. (+info)Transient leukoerythroblastosis in a very low birth weight infant with parvovirus B19 infection. (5/10)
(+info)An unusual case of pycnodysostosis. (6/10)
A 6 year old boy with clinical and radiological features of pycnodysostosis is described. In addition to pycnodysostosis he had a myelophthisic type of anaemia suggesting an overlap with osteopetrosis. (+info)Normoblasts in peripheral blood of Nigerians: their clinical significance. (7/10)
The clinical conditions associated with peripheral blood nucleated red blood cells (NRBC) in Nigerians were investigated prospectively to define them and establish their mortality. Of the 4,565 differential counts carried out within ten months, NRBC were detected in 120 cases (2.6 percent). Of these, severe nutritional anemia was seen in 64.4 percent, sickle cell anemia in 23.8 percent, neonatal status in 7.6 percent; and malignant diseases in 4.2 percent. Leukoerythroblastosis occurred in 11 percent. The overall mortality was 4.2 percent, and among those with congestive cardiac failure, there was no fatality. These results show that malignancy is not a major cause of normoblasts in peripheral blood in this environment and that the prognosis is not as poor as has been reported in some North American and European literature. (+info)Coeliac disease presenting with a leuco-erythroblastic anaemia. (8/10)
A 49-year-old Irishman presented as an emergency with watery diarrhoea and a leuco-erythroblastic anaemia. Investigations showed that he had coeliac disease but no evidence of bone marrow infiltration. His leuco-erythroblastic picture disappeared on treatment with iron and folic acid. (+info)
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What is a word py meaning. Definition of py.
Myelophthisic anemia
... (or myelophthisis) is a severe type of anemia found in some people with diseases that affect the bone ... "Myelophthisic Anemia: Anemias Caused by Deficient Erythropoiesis: Merck Manual Professional". Retrieved 2008-03-08. ... from myelophthisic anemia because in aplastic anemia the hematopoietic cells are damaged and immature blood cells are not seen ... Myelophthisic Anemia at eMedicine (Articles with short description, Short description is different from Wikidata, Aplastic ...
Hypophosphatasia
... resulting in myelophthisic anemia. In radiographic examinations, perinatal hypophosphatasia can be distinguished from even the ...
Plateletpheresis
... those with myelophthisic anemia, AIDS, or with aplastic anemia. If indicated, transfusions (one thrombapheresis concentrate) ... those with aplastic anemia, AIDS, hypersplenism, idiopathic thrombocytopenic purpura (ITP), sepsis, bone marrow transplant, ...
Anemia
Other mechanisms of impaired RBC production Myelophthisic anemia or myelophthisis is a severe type of anemia resulting from the ... Look up anemia in Wiktionary, the free dictionary. Anemia, U.S. National Library of Medicine [About Anemia] (CS1: long volume ... Fanconi anemia is a hereditary disorder or defect featuring aplastic anemia and various other abnormalities. Anemia of kidney ... Anemia of folate deficiency, as with vitamin B12, causes megaloblastic anemia Anemia of prematurity, by diminished ...
List of MeSH codes (C15)
... anemia, pernicious MeSH C15.378.071.307 - anemia, myelophthisic MeSH C15.378.071.363 - anemia, neonatal MeSH C15.378.071.363. ... anemia, refractory MeSH C15.378.190.625.062.080 - anemia, refractory, with excess of blasts MeSH C15.378.190.625.070 - anemia, ... anemia, diamond-blackfan MeSH C15.378.071.085.080.280 - fanconi anemia MeSH C15.378.071.141 - anemia, hemolytic MeSH C15.378. ... anemia, hypochromic MeSH C15.378.071.196.300 - anemia, iron-deficiency MeSH C15.378.071.252 - anemia, macrocytic MeSH C15.378. ...
Anemia of Chronic Disease and Kidney Failure: Overview, Mechanism of Anemia of Chronic Disease, Prevalence of Anemia of Chronic...
... anemia is considered when one or more of the following are decreased: hemoglobin, hematocrit, or red blood cell (RBC) count. ... anemia refers to an absolute reduction of the total number of circulating red blood cells (RBCs). For practical purposes, ... Myelophthisic anemia (see the image below) This blood film at 1000X magnification demonstrates a leukoerythroblastic blood ... How is anemia defined?. What is the etiologic category of anemia of chronic illness and anemia of chronic kidney disease (CKD)? ...
Blood smear: MedlinePlus Medical Encyclopedia
Anemia caused by bone marrow not producing normal blood cells due to toxins or tumor cells (myelophthisic process) ... Congenital hemolytic anemia. *Disorder in which RBCs break down when the body is exposed to certain medicines or is stressed ... Low number of RBCs due to the body destroying them (immune hemolytic anemia) ...
2011 ICD-9-CM Diagnosis Code 285.9 : Anemia unspecified
myelophthisic (normocytic) 284.2. *. newborn (see also Disease, hemolytic) 773.2. *. due to isoimmunization (see also Disease, ... anemia (due to):*blood loss:*acute (285.1. )*chronic or unspecified (280.0. )*iron deficiency (280.0. -280.9. ) ... Short description: Anemia NOS.. *ICD-9-CM 285.9 is a billable medical code that can be used to indicate a diagnosis on a ... Home > 2011 ICD-9-CM Diagnosis Codes > Diseases Of The Blood And Blood-Forming Organs 280-289 > Other and unspecified anemias ...
Myelofibrosis-associated complications: pathogenesis, clinical manifes | IJGM
Currently available therapies have no or limited efficacy in the treatment of MF-related anemia. Thus, management of anemia ... Progressive bone marrow fibrosis leads to a "myelophthisic" phenotype with worsening cytopenias, particularly thrombocytopenia ... The impact of anemia in patients with respiratory failure. Chest. 2005;128(5 Suppl 2):576S-582S. ... Consequently, the rates of grade 3 and 4 events of thrombocytopenia or anemia tend to be highest within the first 8-12 weeks of ...
Fanconi anemia - Wikipedia
Fanconi Anemia~clinical at eMedicine *^ Kutler DI, Auerbach AD (2004). "Fanconi anemia in Ashkenazi Jews". Fam. Cancer. 3 (3-4 ... Fanconi Anemia~treatment at eMedicine *^ Page 29 in Moore, Pete (2007). The Debate About Genetic Engineering (Ethical Debates) ... Fanconi anaemia (FA) is a rare genetic disease resulting in impaired response to DNA damage. Although it is a very rare ... DNA double-strand damages also activate the Fanconi anemia core complex (FANCA/B/C/E/F/G/L/M).[13] The FA core complex ...
Orofacial manifestations of hematological disorders: Anemia and hemostatic disorders Adeyemo TA, Adeyemo WL, Adediran A,...
These features are also seen in secondary thrombocytopenia due to the myelophthisic syndrome, autoimmune disorder, aplastic ... Orofacial Manifestations of Anemia. Iron deficiency anemia. Iron deficiency anemia is the most common hematological disorder. [ ... Mesh phrases used in the search were: oral diseases AND anaemia; orofacial diseases AND anaemia; orofacial lesions AND anaemia ... Mesh phrases used in the search were: oral diseases AND anaemia; orofacial diseases AND anaemia; orofacial lesions AND anaemia ...
What is congenital Dyserythropoietic anemia?
Congenital dyserythropoietic anemia (CDA) is an inherited blood disorder that affects the development of red... ... What is Myelophthisic anemia?. Myelophthisic anemia is anemia characterized by the presence of immature erythrocytes in the ... What causes Myelophthisic anemia?. Myelophthisic anemia is a normocytic, normochromic anemia that occurs when normal marrow ... Vitamin deficiency anemia. ... Anemia of inflammation. ... Aplastic anemia. ... Anemias associated with bone marrow disease ...
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Code System Concept
Myelophthisic anaemia Active Synonym false false 483386018 Anaemia associated with marrow infiltration Active Synonym false ... Anemia associated with marrow infiltration Active Synonym false false 5566013 Leukoerythroblastic anemia Active Synonym false ... Myelophthisic anemia (disorder). Code System Preferred Concept Name. Myelophthisic anemia (disorder). Concept Status. Published ... Myelophthisic anemia Active Synonym false false 5564011 ...
DeCS
Anemias, Myelophthisic. Leukoerythroblastic Anemia. Leukoerythroblastic Anemias. Myelophthisic Anemia. Myelophthisic Anemias. ... Anemias, Leukoerythroblastic Anemias, Myelophthisic Leukoerythroblastic Anemia Leukoerythroblastic Anemias Myelophthisic Anemia ... Anemia, Myelophthisic - Preferred Concept UI. M0001135. Scope note. Anemia characterized by appearance of immature myeloid and ... anemia leucoeritroblástica anemia mielopática Scope note:. Anemia caracterizada por la aparición de eritrocitos inmaduros ...
Primary Myelofibrosis Treatment & Management: Approach Considerations, JAK Inhibitors, FGFR Inhibitors
Of 84 patients with myelofibrosis-associated anemia who were randomized, response in anemia was documented in 20 patients, ... Myelophthisic Anemia Medscape Consult. News & Perspective. * Incyte to Discontinue Late-Stage Trial for Bone Marrow Cancer Drug ... Anemia and thrombocytopenia were the most common adverse events, with 2 patients in ruxolitinib group having transformation to ... Response in leukocytosis, anemia, and thrombocytosis occurred in 15%-25% of patients. Clinical responses were not associated ...
Macrocytosis: Practice Essentials, Pathophysiology, Etiology
Refractory anemias of the following types may cause macrocytosis:. * Myelodysplastic anemias * Myelophthisic anemias (marrow ... The most common cause of macrocytic anemia is megaloblastic anemia, which is the result of impaired DNA synthesis. Although DNA ... In patients with hemolytic anemia or posthemorrhagic anemia, the reticulocyte count increases. The reticulocyte, an immature ... 1] Increased MCV is an indication of macrocytic anemia when any of the following is present [2] :. * In nonpregnant females, ...
Macrocytosis: Practice Essentials, Pathophysiology, Etiology
Refractory anemias of the following types may cause macrocytosis:. * Myelodysplastic anemias * Myelophthisic anemias (marrow ... The most common cause of macrocytic anemia is megaloblastic anemia, which is the result of impaired DNA synthesis. Although DNA ... In patients with hemolytic anemia or posthemorrhagic anemia, the reticulocyte count increases. The reticulocyte, an immature ... 1] Increased MCV is an indication of macrocytic anemia when any of the following is present [2] :. * In nonpregnant females, ...
Metastatic Bone Disease Treatment & Management: Approach Considerations, Spinal Radiation Therapy, Pharmacologic Therapy
Pesquisa | Biblioteca Virtual em Saúde - BRASIL
Metastasis to bone marrow with myelophthisic anemia is especially rare. To our knowledge, there have been only 5 reported cases ... Case of metastatic basal cell carcinoma to bone marrow, resulting in myelophthisic anemia. ... Anemia Mielopática/etiologia , Neoplasias da Medula Óssea/complicações , Neoplasias da Medula Óssea/secundário , Carcinoma ... Laboratory findings were notable for normocytic anemia, thrombocytopenia, and elevated LDH. Further work up with bone marrow ...
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Anemia, Aplastic | Profiles RNS
Anemia, Hypochromic. *Anemia, Macrocytic. *Anemia, Myelophthisic. *Anemia, Neonatal. *Anemia, Refractory. *Anemia, ... A form of anemia in which the bone marrow fails to produce adequate numbers of peripheral blood elements. ... Cai B, Said Q, Li X, Li FY, Arcona S. Healthcare resource use and direct costs in severe aplastic anemia (SAA) patients before ... Cai B, Said Q, Li X, Li FY, Arcona S. Healthcare costs and resource utilization in patients with severe aplastic anemia in the ...
Erythrocyte Morphology on Peripheral Smear
Hemolytic Anemia Purpura Thrombotic Thrombocytopenic Purpura Sideroblastic Anemia Hereditary Spherocytosis Hemolytic Anemia ... Acute Kidney Injury Anemia Evaluation Red Blood Cell Peripheral Smear Asplenic Primary Immunodeficiency Macrocytic Anemia ... An abnormally large red blood cell occurring mainly in anemias (as pernicious anemia), also called megalocyte. Lack of vitamin ... Anatomy Chapter Anemia Chapter Bone Marrow Disorders Chapter Cancer Chapter Cardiovascular Medicine Chapter Coagulopathy ...
Fast Five Quiz: Imaging Studies in Metastatic Bone Disease
DEPARTMENT OF HAEMATOLOGY - Basic Medical Sciences
anaemia).. Anaemia due to bone marrow failure:. Myelophthisic anaemia, Aplastic anaemia.. Haemolytic anaemia: due to ... Microcytic anaemia: Iron deficiency, lead poisoning, thalassemia and anaemia of. chronic disorders.. Macrocytic anaemia:. ... Acquired haemolytic anaemia. Immune haemolytic anaemia due to antibodies (idiopathic, Evans syndrome,. cold agglutinin ... Abnormal RBC morphology in anaemia.. Systematic plan for the diagnosis of anaemia.. Indication for bone marrow aspiration and ...
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Anemia, Sideroblastic | Profiles RNS
Anemia, Hypochromic. *Anemia, Macrocytic. *Anemia, Myelophthisic. *Anemia, Neonatal. *Anemia, Refractory. *Anemia, ... "Anemia, Sideroblastic" is a descriptor in the National Library of Medicines controlled vocabulary thesaurus, MeSH (Medical ... Anemia characterized by the presence of erythroblasts containing excessive deposits of iron in the marrow. ... This graph shows the total number of publications written about "Anemia, Sideroblastic" by people in this website by year, and ...
Role of Chronic Iron Overload in Multiple Disorders of Captive Black Rhinoceroses (Diceros bicornis) - AAZV 1999 - VIN
This group also had high incidences of primary hemolytic anemia and mucocutaneous ulcerative disease. Open symbols in Group B ... producing in some instances a myelophthisic siderosis. ... These include episodic hemolytic anemia; high susceptibility to ... chronic progressive anemia with severe weight loss and occult infection; and a more recently recognized syndrome involving the ... dying in captivity have frequently cited hemosiderosis as residual evidence of hemolytic anemia, a disorder of high morbidity ...
Lead Poisoning - Hematology - Medbullets Step 1Leukoerythroblastic1
- Leukoerythroblastic anemia in metastatic prostate cancer. (medscape.com)
Hemolytic4
- Patients with myelophthisic anemia secondary to cobalamin deficiency may also present with leukoerythroblastosis, a hemolytic picture, and splenomegaly. (medscape.com)
- Go to Anemia , Chronic Anemia , Megaloblastic Anemia , Hemolytic Anemia , and Sideroblastic Anemias for complete information on these topics. (medscape.com)
- Hemolytic anemias. (psichologyanswers.com)
- Necropsy reports of black rhinoceroses ( Diceros bicornis ) dying in captivity have frequently cited hemosiderosis as residual evidence of hemolytic anemia, a disorder of high morbidity and mortality in this species. (vin.com)
Aplastic anemia5
- Among those affected, the majority develop cancer , most often acute myelogenous leukemia (AML), and 90% develop aplastic anemia (the inability to produce blood cells) by age 40. (wikipedia.org)
- Anemic disorders associated with orofacial signs and symptoms include iron deficiency anemia, Plummer-Vinson syndrome, megaloblastic anemia, sickle cell anemia, thalassaemia and aplastic anemia. (ijdr.in)
- Aplastic anemia. (psichologyanswers.com)
- Cai B, Said Q, Li X, Li FY, Arcona S. Healthcare resource use and direct costs in severe aplastic anemia (SAA) patients before and after treatment with eltrombopag. (uams.edu)
- Aplastic Anemia in Two Patients with Sex Chromosome Aneuploidies. (uams.edu)
Disorder3
- Iron deficiency anemia is the most common hematological disorder. (ijdr.in)
- Congenital dyserythropoietic anemia (CDA) is an inherited blood disorder that affects the development of red blood cells. (psichologyanswers.com)
- This disorder is one of many types of anemia , which is a condition characterized by a shortage of red blood cells. (psichologyanswers.com)
Normochromic2
- When the classification of anemia is based on the morphology of the RBCs, both anemia of chronic illness and anemia of CKD usually fall under the classification of normochromic, normocytic anemia. (medscape.com)
- Myelophthisic anemia is a normocytic, normochromic anemia that occurs when normal marrow space is infiltrated and replaced by nonhematopoietic or abnormal cells. (psichologyanswers.com)
Secondary3
- Generally, in myelophthisic anemia, a form of fibrosis, occurs secondary to injury by nonhematopoietic cells or pathogens. (medscape.com)
- The prevalence of anemia is lower in current smokers, which has been attributed to secondary erythrocytosis. (medscape.com)
- Patients with myeloma, leukemia, or metastatic carcinoma may have anemia, thrombocytopenia, and leukopenia secondary to chronic disease and marrow replacement. (medscape.com)
Diagnosis2
- anemia itself should not be considered a diagnosis. (medscape.com)
- Systematic plan for the diagnosis of anaemia. (uniben.edu)
Marrow9
- Pham CM, Syed AA, Siddiqui HA, Keller RA, Kowalewski C. Case of metastatic basal cell carcinoma to bone marrow, resulting in myelophthisic anemia. (medscape.com)
- Infiltrating lesions caused by nonhematopoietic cells invading bone marrow can result in varying degrees of cytopenia, including anemia , thrombocytopenia, neutropenia, and pancytopenia. (medscape.com)
- Myelophthisic anemia is anemia characterized by the presence of immature erythrocytes in the peripheral blood due to the infiltration (crowding out) of the bone marrow by abnormal tissue. (psichologyanswers.com)
- Hypoproliferative anemia results from the inability of bone marrow to produce adequate numbers of red blood cells. (psichologyanswers.com)
- The list of conditions that cause hypoproliferative anemia is long, starting from common etiologies as iron deficiency to rarer diagnoses of constitutional bone marrow failure syndromes. (psichologyanswers.com)
- Anemias associated with bone marrow disease. (psichologyanswers.com)
- Anemia characterized by appearance of immature myeloid and nucleated erythrocytes in the peripheral blood, resulting from infiltration of the bone marrow by foreign or abnormal tissue. (bvsalud.org)
- A form of anemia in which the bone marrow fails to produce adequate numbers of peripheral blood elements. (uams.edu)
- Anemia characterized by the presence of erythroblasts containing excessive deposits of iron in the marrow. (ouhsc.edu)
Sickle cell a1
- Sickle cell anemia. (psichologyanswers.com)
RBCs1
- By definition, anemia refers to an absolute reduction of the total number of circulating red blood cells (RBCs). (medscape.com)
Microcytic1
- Microcytic anaemia: Iron deficiency, lead poisoning, thalassemia and anaemia of chronic disorders. (uniben.edu)
Severe3
- [1] The well-known cancer susceptibility genes BRCA1 and BRCA2 are also examples of FA genes (FANCS and FANCD1 respectively), and biallelic mutation of any of the two genes usually results in an embryonically lethal outcome, and should the proband come to term, experience a severe form of Fanconi anemia. (wikipedia.org)
- Severe anemia is treated with a blood transfusion of red blood cells, no matter what the cause is. (psichologyanswers.com)
- What level of anemia is severe? (psichologyanswers.com)
Congenital3
- What is congenital Dyserythropoietic anemia? (psichologyanswers.com)
- How is congenital Dyserythropoietic anemia treated? (psichologyanswers.com)
- Congenital Dyserythropoietic Anemia (CDA) Type 2 is the most common and type 3 is the rarest. (psichologyanswers.com)
Patients2
- However, in patients with chronic kidney disease (CKD), the risk of developing anemia is 30% higher in males than in females. (medscape.com)
- Anemia is common in patients with CKD. (medscape.com)
Chronic10
- Anemia may arise as a complication of several chronic diseases, and chronic kidney disease (CKD) in particular. (medscape.com)
- See Anemia and Chronic Kidney Disease for more complete information on those topics. (medscape.com)
- For patient education information, see Anemia and Chronic Kidney Disease , as well as the National Kidney Foundation's Anemia and Chronic Kidney Disease . (medscape.com)
- Anemia of chronic illness traditionally encompassed any inflammatory, infectious, or malignant disease of a long-standing nature. (medscape.com)
- Another proposed mechanism for anemia of chronic illness involves cytokines, such as interleukins (IL-1 and IL-6) and tumor necrosis factor (TNF-alpha). (medscape.com)
- Why does chronic disease cause anemia? (psichologyanswers.com)
- Is chronic anemia curable? (psichologyanswers.com)
- How is chronic anemia treated? (psichologyanswers.com)
- What is the treatment for anemia of chronic disease? (psichologyanswers.com)
- Anemia can occur due to blood loss or to certain chronic medical conditions or nutritional deficiencies. (psichologyanswers.com)
Morphology1
- Abnormal RBC morphology in anaemia. (uniben.edu)
Hemoglobin3
- For practical purposes, anemia is considered when one or more of the following are decreased: hemoglobin concentration, hematocrit, or RBC count. (medscape.com)
- Mild anemia corresponds to a level of hemoglobin concentration of 10. (psichologyanswers.com)
- With anemia, the heart must work harder to make up for the lack of red blood cells or hemoglobin. (psichologyanswers.com)
Erythropoietin1
- The severity of anemia of CKD is directly related to the degree of loss of kidney function, as the kidneys are responsible for approximately 90% of erythropoietin production. (medscape.com)
Descriptor1
- Anemia, Aplastic" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings) . (uams.edu)
Deficiency7
- Hemodialysis to treat CKD may also lead to iron-deficiency anemia. (psichologyanswers.com)
- People with IBD may have both iron-deficiency anemia due to blood loss and anemia of inflammation. (psichologyanswers.com)
- A poor diet or certain intestinal diseases that affect how the body absorbs iron can also cause iron deficiency anemia. (psichologyanswers.com)
- Vitamin deficiency anemia. (psichologyanswers.com)
- If left untreated, iron-deficiency anemia can cause serious health problems. (psichologyanswers.com)
- Iron-deficiency anemia develops slowly - your symptoms could be mild, or you may not even have any. (psichologyanswers.com)
- Megaloblastic anaemia: Folic acid deficiency, vitamin B12 (including Pernicious anaemia). (uniben.edu)
Hematological3
- The aim of this paper is to review the literature and identify orofacial manifestations of hematological diseases, with particular reference to anemias and disorders of hemostasis. (ijdr.in)
- A computerized literature search using MEDLINE was conducted for published articles on orofacial manifestations of hematological diseases, with emphasis on anemia. (ijdr.in)
- In this review of orofacial manifestations of hematological disorders, orofacial manifestations of anemia and disorders of hemostasis are discussed. (ijdr.in)
Immune1
- Immune haemolytic anaemia due to antibodies (idiopathic, Evans syndrome, cold agglutinin antibodies, paroxysmal cold haemoglobinuria (PCH) and drug- induced immune haemolytic anaemia. (uniben.edu)
Classification1
- Definitions and classification of anaemia I. (uniben.edu)
Pallor1
- Anemia may cause skin pallor. (medscape.com)
Iron1
- This most common type of anemia is caused by a shortage of iron in your body. (psichologyanswers.com)
Lack1
- Does lack of sleep cause anemia? (psichologyanswers.com)
Blood loss1
- Anemia usually is grouped into three etiologic categories: decreased RBC production, increased RBC destruction, and blood loss. (medscape.com)
Produce1
- Anemia caracterizada por la aparición de eritrocitos inmaduros mieloides y nucleados en la sangre periférica, que se produce debido a la infiltración de la médula ósea por tejido extraño o anormal. (bvsalud.org)
Cells1
- Causes of anemia in CKD may include inflammation, low levels of EPO due to kidney damage, or low levels of the nutrients needed to make red blood cells. (psichologyanswers.com)
General1
- Anemia in general causes 1. (psichologyanswers.com)
Damage1
- Fanconi anaemia ( FA ) is a rare genetic disease resulting in impaired response to DNA damage. (wikipedia.org)
Type1
- What is the rarest type of anemia? (psichologyanswers.com)
Present1
- About 2% of FA cases are X-linked recessive, which means that if the mother carries one mutated Fanconi anemia allele on one X chromosome , a 50% chance exists that male offspring will present with Fanconi anemia. (wikipedia.org)
People2
- This graph shows the total number of publications written about "Anemia, Aplastic" by people in UAMS Profiles by year, and whether "Anemia, Aplastic" was a major or minor topic of these publications. (uams.edu)
- Below are the most recent publications written about "Anemia, Aplastic" by people in Profiles over the past ten years. (uams.edu)
