| elliptocytary anaemia | Anaemia with elliptocytosis; a heterogeneous group of inherited anaemias having in common elliptical red cells on blood smear. The defect may reside in dysfunction or deficiency of proteins of the red cell membrane skeleton. Synonym: elliptocytotic anaemia. (05 Mar 2000) |
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| elliptocytic anaemia | Anaemia characterised by elliptical erythrocytes (ovalocytes) resembling those observed normally in camels; 1 to 15% of erythrocytes in nonanaemic persons may be oval, but greater proportions are observed in certain patients with microcytic anaemia. See: elliptocytosis. Synonym: cameloid anaemia, ovalocytic anaemia. (05 Mar 2000) |
| elliptocytotic anaemia | Anaemia with elliptocytosis; a heterogeneous group of inherited anaemias having in common elliptical red cells on blood smear. The defect may reside in dysfunction or deficiency of proteins of the red cell membrane skeleton. Synonym: elliptocytotic anaemia. (05 Mar 2000) |
| toxic anaemia | Any anaemia resulting from the destructive effects of a chemical, metabolic poison, bacterial toxin, venom, and similar materials. (05 Mar 2000) |
| traumatic anaemia | An acute anaemia caused by fairly sudden and rapid loss of blood, as by traumatic laceration of a relatively large vessel, erosion of an artery in a duodenal ulcer, haemorrhage in an ectopic pregnancy, or the result of such diseases as haemophilia and acute leukaemia. Synonym: traumatic anaemia. (05 Mar 2000) |
| equine infectious anaemia | <veterinary> virology> Viral disease of horses caused by the equine infectious anaemia virus (eiav; infectious anaemia virus, equine). It is characterised by intermittent fever, weakness, and anaemia. Chronic infection consists of acute episodes with remissions. (12 Dec 1998) |
| equine infectious anaemia virus | <virology> A retrovirus, of the Lentivirinae subfamily, and the cause of equine infectious anaemia. Synonym: swamp fever virus. (05 Mar 2000) |
| tropical anaemia | Various syndromes frequently observed in persons in tropical climates, usually resulting from nutritional deficiencies or hookworm or other parasitic diseases. (05 Mar 2000) |
| erythroblastic anaemia | Anaemia characterised by the presence of large numbers of nucleated red cells (normoblasts and erythroblasts) in the peripheral blood. Seen especially in newborns with haemolytic anaemia, such as that caused by Rh or ABO incompatibility. Synonym: erythroblastic anaemia. (05 Mar 2000) |
| erythronormoblastic anaemia | Anaemia characterised by the presence of large numbers of nucleated red cells (normoblasts and erythroblasts) in the peripheral blood. Seen especially in newborns with haemolytic anaemia, such as that caused by Rh or ABO incompatibility. Synonym: erythroblastic anaemia. (05 Mar 2000) |
| Faber's anaemia | A form of chronic hypochromic microcytic anaemia associated with achlorhydria or achylia gastrica; observed most frequently in women in the third to fifth decades. Synonym: Faber's anaemia, Faber's syndrome. (05 Mar 2000) |
| false anaemia | Pallor of the skin and mucous membranes without the blood changes of anaemia. Synonym: false anaemia. (05 Mar 2000) |
| familial erythroblastic anaemia | An outmoded term for thalassaemia major. (05 Mar 2000) |
| familial hypoplastic 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) |
| familial microcytic anaemia | A rare type of autosomal recessive hypochromic microcytic anaemia associated with a defect of iron metabolism characterised by high serum iron, hepatic iron deposits, and absence of stainable bone marrow iron stores. (05 Mar 2000) |