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"endothelial dystrophy of cornea"¿¡ ´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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  • ¿µ¹®
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  • hereditary macular dystrophy
    À¯Àü¼ºÈ²¹ÝÀÌ¿µ¾ç(Áõ)
  • infantile neuroaxonal dystrophy
    ¿µ¾Æ½Å°æÃà»è¼º ÀÌ¿µ¾çÁõ, »çÀÌÅйö°Å¾¾º´.
  • 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)
  • macular corneal dystrophy
    ¹ÝÁ¡°¢¸·ÀÌ¿µ¾çÁõ.
  • macular corneal dystrophy
    ¹ÝÁ¡°¢¸·ÀÌ¿µ¾ç(Áõ)
  • map-dot-fingerprint dystrophy
    ¹«´Ì°¢¸·ÀÌ¿µ¾ç(Áõ), ¹®¾ç°¢¸·ÀÌ¿µ¾ç(Áõ)
  • median nail dystrophy
    Á¤Áß¼Õ¹ßÅéÀÌ¿µ¾ç(Áõ)
  • metachromatic dystrophy
    ÀÌ¿°¼º ÀÌ¿µ¾çÁõ(ì¶æøàõì¶ç½å×ñø).
  • metachromatic dystrophy
    ÀÌ¿°¼º ÀÌ¿µ¾çÁõ(¡­ì¶ç½å×ñø)
  • microcystic corneal dystrophy
    ¼Ò³¶Æ÷°¢¸·ÀÌ¿µ¾ç(Áõ)
  • muscle dystrophy
    ±ÙÀÌ¿µ¾çÁõ.
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APECED Autoimmune Poly-Endocrinopathy Candidiasis Ectodermal Dystrophy
DMD Duchenne type Muscular Dystrophy; ¾Ç¼ºÇü DuchenneÇü ±ÙÀÌ¿µ¾çÁõ
MLD Metachromatic Leuko-Dystrophy
RSDS Reflex Sympathetic Dystrophy Syndrome
ADT Accepted Dental Therapeutics; adenosine triphosphate; admission, discharge, transfer; agar-gel diffu...
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SCARMD Severe childhood autosomal recessive muscular dystrophy
SFD Sorsby fundus dystrophy
CRD cone-rod dystrophy
DM-PK dystrophy protein kinase
ABAE Adult bovine aortic endothelial
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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' 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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