- nonspherocytic hemolytic anemia
- see congenital nonspherocytic hemolytic a.
Medical dictionary. 2011.
nonspherocytic hemolytic anemia
Look at other dictionaries:
hemolytic anemia — n anemia caused by excessive destruction (as in chemical poisoning, infection, or sickle cell anemia) of red blood cells * * * any of a group of acute or chronic anemias characterized by excessive hemolysis (shortened survival of mature… … Medical dictionary
Congenital hemolytic anemia — Classification and external resources ICD 10 D55 D58 ICD 9 … Wikipedia
congenital nonspherocytic hemolytic anemia — any of a heterogeneous group of inherited anemias characterized by shortened red blood cell survival, lack of spherocytosis, and normal osmotic fragility associated with erythrocyte membrane defects, multiple intracellular enzyme deficiencies or… … Medical dictionary
PKLR — Pyruvate kinase, liver and RBC, also known as PKLR, is a human gene.cite web | title = Entrez Gene: PKLR pyruvate kinase, liver and RBC| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=5313| accessdate = ]… … Wikipedia
Adenylate kinase — 3D ribbon/surface model of adenylate kinase in complex with bis(adenosine)teraphosphate (ADP ADP) Identifiers Symbol ADK … Wikipedia
GPI (gene) — Glucose phosphate isomerase, also known as GPI, is a human protein encoded by the gene|GPI gene.cite web | title = Entrez Gene: GPI glucose phosphate isomerase| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView… … Wikipedia
deficiency — An insufficient quantity of some substance (as in dietary d. or hemoglobin d. in marrow aplasia); organization (as in mental d.); activity (as in enzyme d. or reduced oxygen carrying capacity of the blood), etc., of which the amount present is of … Medical dictionary
Hemoglobin — The oxygen carrying pigment and predominant protein in the red blood cells. Hemoglobin forms an unstable, reversible bond with oxygen. In its oxygenated state it is called oxyhemoglobin and is bright red. In the reduced state it is called… … Medical dictionary
HK1 — Hexokinase 1, also known as HK1, is a human gene. PBB Summary section title = summary text = Hexokinases phosphorylate glucose to produce glucose 6 phosphate, thus committing glucose to the glycolytic pathway. This gene encodes a ubiquitous form… … Wikipedia
НЕДОСТАТОЧНОСТЬ ФЕРМЕНТОВ — мед. Синдромы врождённых нарушений обмена веществ встречаются редко, но оказывают значительное влияние на физическое, интеллектуальное, психическое развитие и качество жизни (например, фенилкетонурия, гомоцистинурия, гликогенозы, синдромы ломкой… … Справочник по болезням
