| 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) |
| primary idiopathic 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) |
| primary macular atrophy of skin | 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) |
| scapulohumeral atrophy | Progressive spinal muscular atrophy beginning in the shoulder. Synonym: scapulohumeral atrophy. (05 Mar 2000) |
| Hoffmann's 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) |
| pulp atrophy | Diminution in size and/or cellular elements of the dental pulp due to interference with the blood supply. (05 Mar 2000) |
| horizontal atrophy | A progressive loss of alveolar and supporting bone surrounding the teeth, beginning at the most coronal level of the bone. Synonym: horizontal resorption. (05 Mar 2000) |
| senile atrophy | Wasting of tissues and organs with advancing age from decreased catabolic or anabolic processes, at times due to endocrine changes, decreased use, or ischemia. Synonym: geromarasmus. (05 Mar 2000) |
| serous atrophy | A degenerative change occurring in fat cells, the fat being absorbed and its place being taken by a serous fluid. (05 Mar 2000) |
| Hunt's atrophy | An obsolete term for atrophy of the small muscles of the hand without sensory disturbances; two types are recognised: thenar, from compression of the thenar branch of the median nerve; hypothenar, from compression of the deep palmar branch of the ulnar nerve. (05 Mar 2000) |
| spinal muscular atrophy | <radiology> 2nd most common autosomal recessive disease in Caucasians, pathology, degeneration of the spinal anterior horn cells, atrophy and wasting of skeletal muscles, types, SMA I = Werdnig-Hoffman disease: rapidly progressive, SMA II = intermediate form, SMA III = Kugelberg-Welander disease: slowly progressive, uncommon adult forms, usual presentations, floppy baby, arthrogryposis, muscle weakness in infancy, diagnosis, weakness and wasting with areflexia, electrophysiology shows anterior horm cell disease, genetics, linked to chromosome 5q., neuronal apoptosis inhibitory protein (NAIP) gene, survival motor neuron (SMN) gene (12 Dec 1998) |