| BDM | Becker's muscular dystrophy |
|---|---|
| BMD | Becker's muscular dystrophy; Boehringer Mannheim Diagnostics; bone marrow depression; bone mineral d... |
| CASMD | congenital atonic sclerotic muscular dystrophy |
| CMS | children's medical services; Christian Medical Society; chronic myelodysplastic syndrome; chromosome... |
| COD-MD | cerebro-ocular dysplasia-muscular dystrophy [syndrome] |
| exhaustion atrophy | Atrophy, especially of glandular cells, believed to result from excessive functional activity or overstimulation. (05 Mar 2000) |
|---|---|
| facioscapulohumeral atrophy | A relatively benign type of muscular dystrophy commencing in childhood and slowly progressive; characterised by wasting and weakness, sometimes asymmetrical, mainly of the muscles of the face, shoulder girdle, and arms; autosomal dominant inheritance. Synonym: facioscapulohumeral atrophy, Landouzy-Dejerine dystrophy. (05 Mar 2000) |
| facioscapulohumeral muscular dystrophy | A relatively benign type of muscular dystrophy commencing in childhood and slowly progressive; characterised by wasting and weakness, sometimes asymmetrical, mainly of the muscles of the face, shoulder girdle, and arms; autosomal dominant inheritance. Synonym: facioscapulohumeral atrophy, Landouzy-Dejerine dystrophy. (05 Mar 2000) |
| yellow atrophy of the liver | See: acute yellow atrophy of the liver. (05 Mar 2000) |
| Kienbock's atrophy | Acute atrophy of bone in an extremity following inflammation. (05 Mar 2000) |
| fatty atrophy | Fatty infiltration secondary to an atrophy of the essential elements of an organ or tissue. (05 Mar 2000) |
| Zimmerlin's atrophy | A variety of hereditary progressive muscular atrophy in which the atrophy begins in the upper half of the body. (05 Mar 2000) |
| Leber's hereditary optic atrophy | Hereditary degeneration of the optic nerve and papillomacular bundle with resulting rapid loss of central vision, progressive for several weeks, then usually stationary with permanent central scotoma; age of onset is variable, most often in the third decade; more males than females are affected and transmission is cytoplasmic and strictly on the female side. Mutation on the mitochondrial chromosome involved, which presumably interacts with an X-linked mutant. This mechanism may explain the bizarre sex ratio, which differs significantly from one country to another. (05 Mar 2000) |
| Leyden-Mobius 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) |
| limb-girdle 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) |
| linear atrophy | Bands of thin wrinkled skin, initially red but becoming purple and white, which occur commonly on the abdomen, buttocks, and thighs at puberty and/or during and following pregnancy, and result from atrophy of the dermis and overextension of the skin; also associated with ascites and Cushing's syndrome. Synonym: atrophoderma striatum, lineae albicantes, lineae atrophicae, linear atrophy, stretch marks, stria, striae atrophicae, striate atrophy of skin, traction atrophy, vergeture. (05 Mar 2000) |
| longitudinal layer of muscular coat | The outer, longitudinal layer of the smooth muscle of the muscular coat. Nomina Anatomica lists longitudinal layers of muscular coats (stratum longitudinale tunicae muscularis...) of the following: 1) colon (... Coli ); 2) rectum (... Recti ); 3) small intestine (... Intestini tenuis ); 4) stomach (... Gastrici ). Synonym: stratum longitudinale tunicae muscularis gastricae, stratum longitudinale tunicae muscularis. (05 Mar 2000) |
| longitudinal layers of muscular tunics | See: longitudinal layer of muscular coat. (05 Mar 2000) |
| accessory portion of spinal accessory nerve | <anatomy, nerve> The roots of the accessory nerve which arise from the medulla; the nerve fibres of the cranial root join the intracranial portion of the vagus nerve and are distributed to the pharyngeal plexus, providing the motor innervation of the soft palate (except the tensor veli palati) and the pharynx. Synonym: pars vagalis nervi accessorii, radices craniales, accessory portion of spinal accessory nerve, cranial roots, vagal part of accessory nerve, vagal part. (05 Mar 2000) |
| acute spinal cord compression | <radiology> Signs and symptoms of cord compression show progression within 24 hours or less: pain, weakness, autonomic dysfunction, sensory loss, ataxia Diagnostic considerations: Primary or secondary malignancy of epidural space or vertebrae, Trauma, Inflammatory process, Osteoarthritis REF: MacNeil BJ, Abrams HL. Brigham and Women's Hospital Handbook of Diagnostic Imaging. Chapter 35. (12 Dec 1998) |