| MLF | Median Longitudinal Fasciculus Role; links the CN III Nucleus with Contralateral CN ... |
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| AMN | adrenomyeloneuropathy; alloxazine mononucleotide; aminonucleoside; anterior median nucleus |
| CD50 | median curative dose |
| CM | California mastitis [test]; calmodulin; capreomycin; carboxymethyl; cardiac murmur; cardiac muscle; ... |
| DSL | M-U distal sensory latency-m-median-ulnar |
| free border of nail | The distal border of the nail that overhangs the tip of the digit. Synonym: margo liber unguis. (05 Mar 2000) |
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| fungal nail infection | The most common fungus infection of the nail is onychomycosis. Onychomycosis makes the nails look white and opaque, thickened, and brittle. Older women (perhaps because oestrogen deficiency may increase the risk of infection) and men and women with diabetes or disease of the small blood vessels (peripheral vacscular disease) are at increased risk. Artificial nails (acrylic or wraps ) increase the risk because when an artificial nail is applied, the nail surface is usually abraded with an emery board damaging it, emery boards can carry infection, and water can collect under the nail creating a moist, warm environment for fungal growth. Alternative names include tinea unguium and ringworm of the nails. (12 Dec 1998) |
| adiposogenital dystrophy | A disorder characterised primarily by obesity and hypogonadotrophic hypogonadism in adolescent boys; dwarfism is rare, and when present is thought to reflect hypothyroidism. Visual loss, behavioural abnormalities, and diabetes insipidus may occur. Frohlich's syndrome often is used synonymously for this disorder, although the original case involved a pituitary tumour; most cases are thought to result from hypothalamic dysfunction in areas regulating appetite and gonadal development. The most common causes are pituitary and hypothalamic neoplasms. Synonym: adiposis orchica, adiposogenital degeneration, adiposogenital dystrophy, adiposogenital syndrome, hypophysial syndrome, hypothalamic obesity with hypogonadism. Origin: L. Fr. G. Dys-, bad, + trophe, nourishment (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) |
| anterior median fissure of medulla oblongata | The longitudinal groove in the midline of the anterior aspect of the medulla oblongata; it is the medullary equivalent of the anterior median fissure of the spinal cord and ends at the foramen caecum posterius; its caudal part is obliterated by the decussation of the pyramids. Synonym: fissura mediana anterior medullae oblongatae, anteromedian groove. (05 Mar 2000) |
| anterior median fissure of spinal cord | A deep median fissure on the anterior surface of the spinal cord. Synonym: fissura mediana anterior medullae spinalis, anteromedian groove, sulcus ventralis. (05 Mar 2000) |
| anterior median line | The line of intersection of the midsagittal plane with the anterior surface of the body. Synonym: linea mediana anterior. (05 Mar 2000) |
| Barnes' dystrophy | A rare type of muscular dystrophy, in which muscles are often hypertrophic and stronger than normal, but later become weak and atrophic. (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) |
| macular dystrophy | A group of disorders involving predominately the posterior portion of the ocular fundus, due to degeneration in the sensory layer of the retina, retinal pigment epithelium, Bruch's membrane, choroid, or a combination of these tissues. See: Stargardt's disease, Best's disease. (05 Mar 2000) |
| palmar branch of median nerve | <anatomy, nerve> Branch of median nerve arising proximal to flexor retinaculum and running superficial to it to supply skin of proximal central palm and thenar eminence. Since it does not traverse carpal tunnel, it is not affected by carpal tunnel syndrome, even though it supplies skin distal to carpal tunnel. Synonym: ramus palmaris nervi mediani. (05 Mar 2000) |
| map-dot-fingerprint dystrophy | Fingerprint dystrophy accompanied by map-like patterns and microcystic epithelial inclusions. (05 Mar 2000) |