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"macular dystrophy"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
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  • facioscapulohumeral muscular dystrophy
    ¾È¸é°ß°©»ó¿Ï±ÙÀÌ¿µ¾çÁõ(¡­ì¶ç½å×ñø).
  • fascioscapulohumeral muscular dystrophy
    ¾È¸é°ß°©»ó¿Ï±Ù ÀÌ¿µ¾çÁõ
  • fingerprint dystrophy
    Áö¹®»ó(°¢¸·)ÀÌ¿µ¾ç(Áõ)
  • fleck corneal dystrophy
    ¹ÝÁ¡°¢¸·ÀÌ¿µ¾çÁõ
  • granular corneal dystrophy
    °ú¸³°¢¸·ÀÌ¿µ¾çÁõ.
  • hereditary corneal dystrophy
    À¯Àü¼º °¢¸·ÀÌ ¿µ¾çÁõ.
  • hereditary corneal dystrophy
    À¯Àü¼º°¢¸·ÀÌ¿µ¾çÁõ.
  • infantile neuroaxonal dystrophy
    ¿µ¾Æ½Å°æÃà»è¼º ÀÌ¿µ¾çÁõ, »çÀÌÅйö°Å¾¾º´.
  • iridocorneal endothelial dystrophy
    ȫä°¢¸·³»ÇÇÀÌ¿µ¾ç(Áõ)
  • juvenile epithelial corneal dystrophy
    ¿¬¼Ò±â°¢¸·»óÇǼ¼Æ÷ÀÌ¿µ¾ç(Áõ)
  • lattice corneal dystrophy
    °ÝÀÚ°¢¸·ÀÌ¿µ¾ç(Áõ)
  • lattice dystrophy
    °ÝÀÚÀÌ¿µ¾ç(Áõ)
  • limb girdle dystrophy
    Áö´ëÇüÀÌ¿µ¾çÁõ(ò¶Óáû¡ì¶ç½å×ñø).
  • limb-girdle muscular dystrophy
    Áö´ëÇü±ÙÀÌ¿µ¾çÁõ(ò¶ÓáúþÐÉì¶ç½å×ñø)
  • map-dot-fingerprint dystrophy
    ¹«´Ì°¢¸·ÀÌ¿µ¾ç(Áõ), ¹®¾ç°¢¸·ÀÌ¿µ¾ç(Áõ)
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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
CD cadaver donor; canine distemper; canine dose; carbohydrate dehydratase; carbon dioxide; cardiac dise...
CDGG corneal dystrophy Groenouw type, granular
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INAD Infantile neuroaxonal dystrophy
LGMD Limb girdle muscular dystrophy
MD MUSCULAR DYSTROPHY
MD Myotonic Dystrophy
MyD Myotonic Dystrophy
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fleck dystrophy of cornea A bilateral occurrence of subtle spots in the corneal stroma; the spots vary in size and shape, and have sharp margins and clear centres; photophobia may occur; autosomal dominant inheritance.
(05 Mar 2000)
Landouzy-Dejerine 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)
lattice corneal dystrophy A corneal dystrophy due to localised accumulation of amyloid in a reticular pattern; manifest at puberty and progressing slowly until eventually useful vision is lost; autosomal dominant inheritance.
(05 Mar 2000)
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)
Fuchs' epithelial dystrophy Epithelial oedema secondary to endothelial dystrophy of the cornea.
(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)
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