| CA | anterior commissure [Lat. commissura anterior]; calcium antagonist; California [rabbit]; cancer; Can... |
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| DIDMOA | diabetes insipidus-diabetes mellitus-optic atrophy [syndrome] |
| DIDMOAD | diabetis insipidus, diabetes mellitus, otpic atrophy, deafness [syndrome] |
| DIMOAD | diabetes insipidus, diabetes mellitus, optic atrophy, deafness |
| DJOA | dominant juvenile optic atrophy |
| macular atrophy | Atrophoderma in which the skin becomes bag like and wrinkled. Synonym: atrophia maculosa varioliformis cutis, atrophoderma maculatum, macular atrophy, primary idiopathic macular atrophy, primary macular atrophy of skin. Origin: G. Anetos, relaxed, + derma, skin (05 Mar 2000) |
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| gastric atrophy | <gastroenterology> A condition in which the stomach muscles shrink and become weak. It results in a lack of digestive juices. Gastritis: Inflammation of the stomach. (12 Dec 1998) |
| marantic atrophy | <medicine> A wasting of flesh without fever or apparent disease; a kind of consumption; atrophy; phthisis. "Pining atrophy, Marasmus, and wide-wasting pestilence." (Milton) Marasmus senilis [L], progressive atrophy of the aged. Origin: NL, fr. Gr, fr, to quench, as fire; pass, to die away. Source: Websters Dictionary (01 Mar 1998) |
| red atrophy | Atrophy due to destruction of the parenchymatous cells of an organ as a consequence of chronic venous congestion. Synonym: red atrophy. (05 Mar 2000) |
| gingival atrophy | The exposure of root surface by an apical shift in the position of the gingiva. (12 Dec 1998) |
| villous atrophy | Abnormality of the small intestinal mucosa with crypt hyperplasia, resulting in flattening of the mucosa and the appearance of atrophy of villi; clinically seen in malabsorption syndromes such as sprue. (05 Mar 2000) |
| central areolar choroidal atrophy | A slowly progressive pigmentary degeneration in young persons; characterised by black foci closely set together and coalescent at the posterior pole and macular region. Synonym: central areolar choroidal atrophy, central areolar choroidal sclerosis. (05 Mar 2000) |
| pelvofemoral muscular dystrophy | One of the less well-defined types of muscular dystrophy, probably heterogenous in nature. Onset usually in childhood or early adulthood and both sexes affected. Characterised by weakness and wasting, usually symmetrical, of the pelvic girdle muscles, the shoulder girdle muscles, or both, but not the facial muscles. Muscle pseudohypertrophy, heart involvement, and mental retardation are absent. Variable inheritance. Synonym: Leyden-Mobius muscular dystrophy, pelvofemoral muscular dystrophy, scapulohumeral muscular dystrophy. (05 Mar 2000) |
| Vulpian's atrophy | Progressive spinal muscular atrophy beginning in the shoulder. Synonym: scapulohumeral atrophy. (05 Mar 2000) |
| cerebellar atrophy | A degeneration of the cerebellum, particularly the Purkinje cells, as the result of abiotrophy or of toxic agents, as in alcoholism. (05 Mar 2000) |
| periodontal atrophy | Decrease in size and/or cellular elements of the periodontium after it has reached normal maturity. (05 Mar 2000) |
| childhood muscular dystrophy | The most common childhood muscular dystrophy, with onset usually before age 6. Characterised by symmetrical weakness and wasting of first the pelvic and crural muscles and then the pectoral and proximal upper extremity muscles; pseudohypertrophy of some muscles, especially the calf; heart involvement; sometimes mild mental retardation; progressive course and early death, usually in adolescence. X-linked inheritance (affects males and transmitted by females). Synonym: childhood muscular dystrophy, Duchenne's disease, pseudohypertrophic muscular dystrophy. (05 Mar 2000) |
| choroidal vascular atrophy | Atrophy affecting either all choroidal vessels or only the choriocapillaris, occurring either diffusely or confined to the posterior pole of the eye. (05 Mar 2000) |
| gyrate atrophy | Progressive, autosomal recessive, diffuse atrophy of the choroid, pigment epithelium, and sensory retina that begins in childhood. (12 Dec 1998) |
| gyrate atrophy of choroid and retina | A slowly progressive atrophy of the choriocapillaris, pigmentary epithelium, and sensory retina, with irregular confluent atrophic areas and an associated ornithinuria; autosomal recessive inheritance; due to a deficiency of ornithine d-aminotransferase. (05 Mar 2000) |