| FSHSMA | facioscapulohumeral spinal muscular atrophy |
|---|---|
| GA | Gamblers Anonymous; gastric analysis; gastric antrum; general anesthesia; general angiography; gener... |
| GAPO | growth retardation, alopecia, pseudo-anodontia, and optic atrophy [syndrome] |
| HOGA | hyperornithinemia with gyrate atrophy |
| JA | judgment analysis; juvenile atrophy; juxta-articular |
| 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) |
| Pick's atrophy | Circumscribed atrophy of the cerebral cortex. Synonym: lobar sclerosis, progressive circumscribed cerebral atrophy. (05 Mar 2000) |
| Werdnig-Hoffmann muscular atrophy | Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised. Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy. (05 Mar 2000) |
| compensatory atrophy | Atrophy especially of an endocrine organ as a result of its function being assumed by a new source of hormone. (05 Mar 2000) |
| congenital cerebellar atrophy | Familial disorder that causes degeneration of various cells in the cerebellum. Two types are recognised, one in which the granular layer cells degenerate, the other in which the Purkinje cells degenerate. (05 Mar 2000) |
| multiple system atrophy | A name grouping together the four cerebral degenerative diseases of olivopontocerebellar atrophy, shy-drager syndrome, striatonigral degeneration, and one form of parkinson disease, considering them different forms of the same disease process. (12 Dec 1998) |
| muscular atrophy | Derangement in size and number of muscle fibres occurring with aging, reduction in blood supply, or following immobilization, prolonged weightlessness, malnutrition, and particularly in denervation. (12 Dec 1998) |
| muscular atrophy, spinal | Progressive degenerative disorder of motor neurons in the spinal cord, brainstem, and motor cortex, manifested clinically by muscular weakness, atrophy, and corticospinal tract signs in varying combinations. (12 Dec 1998) |
| myopathic atrophy | Muscular atrophy caused by a primary disorder of muscle. (05 Mar 2000) |
| postmenopausal atrophy | Atrophy following menopause, as of the genital organs. (05 Mar 2000) |
| cyanotic 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) |
| cyanotic atrophy of the liver | A sequela of longstanding hepatic congestion due to high pressure in the right atrium as in chronic constrictive pericarditis and severe, protracted right ventricular failure. (05 Mar 2000) |
| pressure atrophy | The wasting of hard or soft tissue resulting from excessive pressure applied to tissue by a denture base. (05 Mar 2000) |