| CML | carboxymethyl lysine; cell-mediated lymphocytotoxicity; cell-mediated lympholysis; central motor lat... |
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| FDC | factor-dependent cell [line]; follicular dendritic cell |
| GPC | gastric parietal cell; gel permeation chromatography; giant papillary conjunctivitis; glycophorin C;... |
| HC | hair cell; hairy cell; handicapped; head circumference; head compression; health care; healthy contr... |
| HEC | hamster embryo cell; Health Education Council; human endothelial cell; hydroxyergocalciferol; hydrox... |
| slaty anaemia | An ash-gray pallor in poisoning from acetanelid or silver (argyria). (05 Mar 2000) |
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| spastic anaemia | Local anaemia resulting from nontransitory contraction of the arterial vessels in the affected region. (05 Mar 2000) |
| spherocytic anaemia | <haematology> A hereditary disorder that leads to a chronic haemolytic anaemia due to an abnormality in the red blood cell membrane. This disorder is caused by a defective gene. Red cells are resistant to stress and rupture easily. Infants may appear jaundiced and pale. Fatigue, weakness and shortness of breath are other symptoms that may be seen in older patients. The spleen may also be enlarged. Treatment includes splenectomy (removal of the spleen). After this is accomplished the life-span of the red blood cells returns to normal. (27 Sep 1997) |
| splenic anaemia | <syndrome> Chronic congestive splenomegaly that occurs primarily in children as a sequel to hypertension in the portal or splenic veins, usually as a result of thrombosis of the veins; anaemia, splenomegaly, and irregular episodes of gastrointestinal bleeding are usually observed, with ascites, jaundice, leukopenia, and thrombocytopenia developing in various conbinations. Synonym: Banti's disease, splenic anaemia. (05 Mar 2000) |
| neonatal anaemia | <haematology> A condition which develops in the foetus due to an incompatibility between the mother's blood type (RH factor) and the baby's. Maternal antibodies, which enter the foetal circulation during delivery attack the baby's red blood cells leading to haemolysis (rupture of the cells). Symptoms include an infant with an enlarged liver and spleen, swelling, jaundice and anaemia. (27 Sep 1997) |
| normochromic anaemia | Any anaemia in which the concentration of haemoglobin in the erythrocytes is within the normal range, i.e., the mean corpuscular haemoglobin concentration is from 32 to 36%. Synonym: isochromic anaemia. (05 Mar 2000) |
| normocytic anaemia | Any anaemia in which the erythrocytes are normal in size, i.e., the mean corpuscular volume ranges from 82 to 92 cu um. (05 Mar 2000) |
| nutritional anaemia | Any anaemia resulting from a dietary deficiency of materials essential to red blood cell formation, e.g., iron, vitamins (especially folic acid), protein. Synonym: deficiency anaemia. (05 Mar 2000) |
| nutritional macrocytic anaemia | Macrocytic, megaloblastic anaemia due to deficiency of either folate or vitamin B12. (05 Mar 2000) |
| deficiency anaemia | Any anaemia resulting from a dietary deficiency of materials essential to red blood cell formation, e.g., iron, vitamins (especially folic acid), protein. Synonym: deficiency anaemia. (05 Mar 2000) |
| Diamond-Blackfan anaemia | Congenital nonregenerative, familial hypoplastic, or pure red cell anaemia; erythrogenesis imperfecta; Diamond-Blackfan syndrome; autosomal recessive normocytic normochromic anaemia resulting from congenital hypoplasia of the bone marrow, which is grossly deficient in erythroid precursors while other elements are normal; anaemia is progressive and severe, but leukocyte and platelet counts are normal or slightly reduced; survival of transfused erythrocytes is normal; minor congenital anomalies are found in some patients. Synonym: congenital nonregenerative anaemia, Diamond-Blackfan anaemia, Diamond-Blackfan syndrome, erythrogenesis imperfecta, familial hypoplastic anaemia, pure red cell anaemia. (05 Mar 2000) |
| dilution anaemia | <medicine> An abnormally watery state of the blood; anaemia. Origin: NL, fr. Gr. "ydwr water + blood. Source: Websters Dictionary (01 Mar 1998) |
| dimorphic anaemia | Anaemia in which two distinct forms of red cells are circulating. (05 Mar 2000) |
| diphyllobothrium anaemia | A rare form of macrocytic anaemia associated with Diphyllobothrium latum infection, especially in Finland. Synonym: fish tapeworm anaemia. (05 Mar 2000) |
| drepanocytic anaemia | <haematology> Disease common in races of people from areas in which malaria is endemic. The cause is a point mutation in the allele that codes for the beta chain of haemoglobin with a substitution of (valine for glutamic acid at position 6. The defective haemoglobin (HbS) crystallizes readily at low oxygen tension. In consequence, erythrocytes from homozygotes change from the normal discoid shape to a sickled shape when the oxygen tension is low and these sickled cells become trapped in capillaries or damaged in transit, leading to severe anaemia. In heterozygotes, the disadvantages of the abnormal haemoglobin are apparently outweighed by increased resistance to Plasmodium falciparum malaria, probably because parasitised cells tend to sickle and are then removed from circulation. Symptoms include joint pain, acute abdominal pain, and ulcerations of the lower extremities. Origin: Gr. Haima = blood (18 Nov 1997) |