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  • albipunctate retinal dystrophy
    ÈòÁ¡¸Á¸·ÀÌ¿µ¾ç(Áõ)
  • basement membrane dystrophy
    ±âÀú¸·ÀÌ¿µ¾ç(Áõ)
  • beckers muscular dystrophy
    º£Ä¿ ±ÙÀÌ¿µ¾çÁõ(¡­ÐÉì£ç½å×ñø)
  • butterfly-shaped retinal dystrophy
    ³ªºñ¸ð¾ç¸Á¸·ÀÌ¿µ¾ç(Áõ), Á¢Çü¸Á¸·ÀÌ¿µ¾ç(Áõ)
  • central areolar choroidal dystrophy
    Á߽ɼº¿øÇü¸Æ¶ô¸·ÀÌ¿µ¾ç(Áõ)
  • cone dystrophy
    ÃßüÀÌ¿µ¾ç(Áõ)
  • cone-rod dystrophy
    Ãßü°£Ã¼ÀÌ¿µ¾ç(Áõ)
  • congenital muscular dystrophy
  • distal muscular dystrophy
    ¿øÀ§±ÙÀÌ¿µ¾çÁõ(êÀêÈÐÉì¶ç½å×ñø).
  • distal muscular dystrophy
    ¿øÀ§ ±Ù ÀÌ¿µ¾çÁõ(êÀêÈÐÉì¶ç½å×ñø).
  • dominant cystoid macular dystrophy
    ¿ì¼º³¶Æ÷Ȳ¹ÝÀÌ¿µ¾ç(Áõ)
  • duchenne muscular dystrophy
    µÚ½Ã¿£´À ±ÙÀ§ÃàÁõ
  • duchenne muscular dystrophy
    µà½Ã¿£Çü ±ÙÀÌ¿µ¾çÁõ(¡­ÐÉì¶ç½å×ñø)
  • dystrophy
    ÀÌ¿µ¾ç
  • dystrophy
    ÀÌ¿µ¾çÁõ(ì¶ç½å×ñø), ¿µ¾ç½ÇÁ¶(ç½å×ã÷ðà), ±â´ÉÀå¾Ö(ѦÒöî¡ ),
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PECAM platelet-endothelial cell adhesion molecule
VEGF vascular endothelial growth factor
ALD Adreno-Leuko-Dystrophy
APECED Autoimmune Poly-Endocrinopathy Candidiasis Ectodermal Dystrophy
DMD Duchenne type Muscular Dystrophy; ¾Ç¼ºÇü DuchenneÇü ±ÙÀÌ¿µ¾çÁõ
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SFD Sorsby fundus dystrophy
CRD cone-rod dystrophy
DM-PK dystrophy protein kinase
ABAE Adult bovine aortic endothelial
AECA Anti-endothelial cell antibodies
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twenty-nail dystrophy Longitudinal ridging of all of the nails; seen in alopecia areata and lichen planus.
(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)
Favre's dystrophy Autosomal recessive bilateral peripheral and central retinoschisis with pigmentary degeneration of the retina, chorioretinal atrophy, vitreous degeneration, and night blindness.
Synonym: Favre's dystrophy.
(05 Mar 2000)
fingerprint dystrophy A condition wherein fine parallel lines in a fingerprint configuration area are seen in the basal epithelial layer and basement membrane of the corneal epithelium.
See: map-dot-fingerprint dystrophy.
(05 Mar 2000)
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)
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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