| ¿µ¹® | muscular dystrophy | ÇÑ±Û | ±ÙÀ°ÅðÇàÀ§Ãà |
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| ¼³¸í | ±Ù¼¶À¯ÀÇ ÆÄ±«·Î ÀÎÇÑ Á¡ÁøÀûÀÎ ±ÙÀ§Ãà°ú Çã¾àÀ» Ư¡À¸·Î ÇÏ´Â ÀÏ·ÃÀÇ ¼±ÃµÀûÀÎ Áúȯ±ºÀ» ÅëÅÐ¾î ¸»ÇÑ´Ù. ´ëÇ¥ÀûÀÎ °æ¿ì°¡ µÚ½¨(Duchenne)ÇüÀ¸·Î ¼º¿°»öü ¿¼ºÀ¯ÀüÀ» Çϸç, ´ë°³ 4 ¼¼À̳»¿¡ ¹ßº´ÇØ Ã»³â±â¸¦ ³Ñ±â´Â °æ¿ì°¡ µå¹°´Ù. Ư¡Àû ¼Ò°ßÀ¸·Î ÀåµýÁö±Ù(gastronemius)ÀÇ °ÅÁþºñ´ë(pseudohypertrophy)(½ÇÁ¦ÀûÀ¸·Î´Â ±ÙÀ§ÃàÀÌ ÀϾÁö¸¸, ±Ù¼¶À¯ ´ë½Å¿¡ Áö¹æ¼¼Æ÷°¡ µé¾îÂ÷ µµ¸®¾î ¸¶Ä¡ ±ÙÀ°ÀÌ Áõ°¡ÇÑ °Íó·³ º¸ÀÌ´Â Çö»ó) ¼Ò°ßÀ» º¼ ¼ö ÀÖ´Ù. |
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| FHC | familial hypercholesterolemia; family health center; Ficoll-Hypaque centrifugation; Fuchs heterochro... |
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| FHI | Fuchs' heterochromic iridocyclitis |
| PMD | Progressive Muscular Dystrophy; ÁøÇ༺ ±ÙÀÌ¿µ¾çÁõ Types of PMD(Progressive Muscular Dystroph... |
| CMD | campomelic dysplasia; camptomelic dwarfism; cartilage matrix deficiency; chief medical director; chi... |
| LCD | coal tar solution [liquor carbonis detergens]; lattice corneal dystrophy; liquid crystal diode; loca... |
| APECED | Autoimmune polyendocrinopathy candidiasis ectodermal dystrophy |
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| BMD | Becker Muscular Dystrophy |
| CHED | Congenital Hereditary Endothelial Dystrophy |
| CMD | Congenital muscular dystrophy |
| CMD | Congenital myotonic dystrophy |
| fuchs' endothelial dystrophy | Disorder caused by loss of endothelium of the central cornea. It is characterised by hyaline endothelial outgrowths on descemet's membrane, epithelial blisters, reduced vision, and pain. (12 Dec 1998) |
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| Fuchs' epithelial dystrophy | Epithelial oedema secondary to endothelial dystrophy of the cornea. (05 Mar 2000) |
| angle of Fuchs | <ophthalmology> A crevice between the ciliary and pupillary zones of the iris formed by atrophy of superficial layers of the iris in the pupillary zone. (05 Mar 2000) |
| Dalen-Fuchs nodules | Collections of epithelial cells lying between Bruch's membrane and the retinal pigment epithelium in sympathetic ophthalmia and rarely in other granulomatous intraocular inflammations. (05 Mar 2000) |
| Fuchs' adenoma | <tumour> A benign epithelial tumour of the non-pigmented epithelium of the ciliary body, rarely exceeding 1 mm in diameter. (05 Mar 2000) |
| Fuchs' black spot | An area of pigment proliferation in the macular region in degenerative myopia. (05 Mar 2000) |
| Fuchs' coloboma | A congenital inferior crescent on the choroid at the edge of the optic disk; not associated with myopia. Synonym: congenital conus. (05 Mar 2000) |
| Fuchs, Ernst | <person> Austrian ophthalmologist, 1851-1930. See: Fuchs' adenoma, angle of Fuchs, Fuchs' heterochromic cyclitis, Fuchs' coloboma, Fuchs' epithelial dystrophy, Fuchs' black spot, Fuchs' spur, Fuchs' stomas, Fuchs' syndrome, Fuchs' uveitis, Dalen-Fuchs nodules. (05 Mar 2000) |
| Fuchs' heterochromic cyclitis | <syndrome> A syndrome characterised by heterochromia of the iris, iridocyclitis, keratic precipitates, and cataract. Synonym: Fuchs' heterochromic cyclitis. (05 Mar 2000) |
| Fuchs' syndrome | <syndrome> A syndrome characterised by heterochromia of the iris, iridocyclitis, keratic precipitates, and cataract. Synonym: Fuchs' heterochromic cyclitis. (05 Mar 2000) |
| Fuchs' uveitis | Anterior uveitis and depigmentation of the iris. Synonym: Fuchs' uveitis. (05 Mar 2000) |
| 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) |
| 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) |
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