| Becker's disease | An obscure South African cardiomyopathy leading to rapidly fatal congestive heart failure and idiopathic mural endomyocardial disease. (05 Mar 2000) |
|---|---|
| becker | <zoology> A European fish (Pagellus centrodontus); the sea bream or braise. Source: Websters Dictionary (01 Mar 1998) |
| becker antigen | bea antigen |
| Becker, J | <person> See: Becker's disease. (05 Mar 2000) |
| Becker, Peter | <person> German geneticist, *1908. See: Becker type tardive muscular dystrophy, Becker type muscular dystrophy. (05 Mar 2000) |
| Becker, Samuel | <person> U.S. Dermatologist, 1894-1964. See: Becker's nevus. (05 Mar 2000) |
| Becker's muscular dystrophy | An X-linked inherited disorder characterised by slowly progressive muscle weakness of the legs and pelvis. Other symptoms and findings include increased difficulty walking, intellectual retardation, fatigue and pseudohypertrophy of the calf muscles. (27 Sep 1997) |
| Becker's nevus | A nevus first seen as an irregular pigmentation of the shoulders, upper chest, or scapular area, gradually enlarging irregularly and becoming thickened and hairy. Synonym: pigmented hair epidermal nevus. (05 Mar 2000) |
| Becker's stain | <technique> For spirochetes, a stain applied to thin films fixed in formaldehyde-acetic acid; preparations are treated successively with tannin, carbolic acid, and carbol fuchsin. (05 Mar 2000) |
| Becker type muscular dystrophy | A muscular dystrophy that has many of the clinical features of Duchenne muscular dystrophy e.g., symmetrical involvement of first the pelvicrural muscles and then the pectoral girdle and proximal upper extremity muscles; pseudohypertrophy, especially of the calf muscles but with a much later age of onset (35-45 years), and more benign course. X-linked inheritance. (05 Mar 2000) |
| Becker type tardive muscular dystrophy | Muscular dystrophy of late onset, often in the second or third decade, with relatively mild course; X-linked recessive inheritance; perhaps allelic with Duchenne's dystrophy, but milder and not a genetic lethal. Compare: Duchenne dystrophy. Synonym: Becker type tardive muscular dystrophy. (05 Mar 2000) |
| aaa disease | Endemic anaemia of ancient Egypt, ascribed in the Papyrus Ebers to intestinal infestation with ancylostoma; now called ancylostomiasis. (05 Mar 2000) |
| ABO haemolytic disease of the newborn | Erythroblastosis foetalis due to maternal-foetal incompatibility with respect to an antigen of the ABO blood group; the foetus possesses A or B antigen which is lacking in the mother, and the mother produces immune antibody which causes haemolysis of foetal erythrocytes. (05 Mar 2000) |
| accumulation disease | A disease characterised by abnormal accumulation of a metabolic product in certain cells and tissues; examples include the mucopolysaccharidoses, lipoidoses. (05 Mar 2000) |
| Acosta's disease | A condition that results from prolonged exposure to high altitude. Symptoms include a continuous dry cough, shortness of breath, poor exercise tolerance, dizziness, headache, sleep difficulty, anorexia, confusion, fatigue and a rapid pulse. Treatment includes the immediate movement to a lower altitude. Prophylaxis has been accomplished successfully with the use of acetazolamide (Diamox). (27 Sep 1997) |