| 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] |
| diffuse gallbladder wall thickening | <radiology> Criterion: gall bladder wall greater than 3 mm may appear thicker due to surrounding ascites, cholecystitis (acute or chronic), non-fasting state, chronic hypoalbuminaemia, hepatitis, congestive heart failure, fat in gall bladder fossa Cf: focal thickening (12 Dec 1998) |
|---|---|
| inflammatory gallbladder disease | <radiology> Post-bulbar ulcer, Crohn disease, TB, Strongyloides, pancreatitis / cholecystitis (12 Dec 1998) |
| empyema of gallbladder | Severe acute cholecystitis with purulent inflammation of the gallbladder. Latent empyema, the presence of pus in a cavity, especially one of the accessory sinuses, unattended by subjective symptoms. Synonym: empyema benignum. Loculated empyema, pyothorax in which pleural adhesions form one or more pockets containing pus. (05 Mar 2000) |
| focal gallbladder wall thickening | <radiology> Primary gall bladder carcinoma, adenomyomatosis / hyperplastic cholecystosis, adenomatous polyps, papillary adenomas, metastatic nodules, cholesterol polyps (associated with acoustic shadowing), metachromatic leukodystrophy (rare!) See also: diffuse thickening (12 Dec 1998) |
| large gallbladder | <radiology> Courvoisier phenomenon, neoplasm of pancreatic head, distal common bile duct, papilla, hydrops, empyema, vagotomy, diabetes (20% of DM patients) Cf: small gall bladder (12 Dec 1998) |
| fossa for gallbladder | A depression on the visceral surface of the liver anteriorly, between the quadrate and the right lobes, lodging the gallbladder. Synonym: fossa vesicae biliaris, gallbladder fossa. (05 Mar 2000) |
| fundus of gallbladder | The wide closed end of the gallbladder situated at the inferior border of the liver. Synonym: fundus vesicae biliaris (felleae). (05 Mar 2000) |
| adult pseudohypertrophic 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) |
| 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 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) |
| benign pseudohypertrophic muscular dystrophy | <neurology> 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. (06 Aug 1998) |
| 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) |
| 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) |
| peroneal muscular atrophy | A group of three familial peripheral neuromuscular disorders, sharing the common feature of marked wasting of the more distal extremities, particularly the peroneal muscle groups, resulting in "stork legs." Two of the three subtypes are hereditary sensorimotor polyneuropathies, one demyelinating in type and the other axon loss in type, while the third subgroup is an anterior horn cell disorder. It usually involves the legs before the arms; pes cavus is often the first sign; autosomal dominant, autosomal recessive, and X-linked recessive types, with severity related to genetic type. Synonym: Charcot-Marie-Tooth disease. (05 Mar 2000) |