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  • central retinal artery
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  • central retinal artery
    ¸Á¸·Á߽ɵ¿¸Æ(ØÑدñéãýÔÑØæ).
  • central retinal artery occlusion
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  • central retinal vein
    ¸Á¸·Áß½ÉÁ¤¸Æ
  • central retinal vein
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  • central retinal vein occlusion
    ¸Á¸·Áß½ÉÁ¤¸ÆÆó¼â
  • complicated retinal detachment
    ÇÕº´¸Á¸·¹Ú¸®
  • congenital retinal fold
    ¼±Ãµ¸Á¸·(¡­ØÑد)ÁÖ¸§.
  • exudative retinal detachment
    »ïÃâ¸Á¸·¹Ú¸®
  • falciform retinal detachment
    ³´¸ð¾ç¸Á¸·¹Ú¸®, °â»ó¸Á¸·¹Ú¸®
  • falciform retinal fold
    ³´¸ð¾ç¸Á¸·ÁÖ¸§, °â»ó¸Á¸·ÁÖ¸§
  • giant retinal tear
    °Å´ë¸Á¸·¿­°ø
  • horseshoe retinal tear
    ¸»¹ß±Á¸ð¾ç¸Á¸·¿­°ø, ¸¶Á¦Çü¸Á¸·¿­°ø
  • hydraulic retinal reattachment
    ¼ö¾ÐÀÌ¿ë¸Á¸·ÀçÀ¯Âø¼ú
  • juvenile recurrent retinal hemorrhage =Eales disease
    ¿¬¼Ò¼º Àç¹ß¼º ¸Á¸·ÃâÇ÷Áõ(¡­î¢Û¡àõØÑدõóúìñø).
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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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MMD Myotonic muscular dystrophy
MyD Myotonic muscular dystrophy
NAD Neuroaxonal dystrophy
OPMD Oculopharyngeal muscular dystrophy
PRA Progressive retinal atrophy
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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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