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"circulatory optic atrophy"¿¡ ´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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  • testicular atrophy
    °íȯÀ§Ãà(ÍÂü¯ê×õê)
  • thenar atrophy
    ¹«Áö±¸À§Ãà(¡­ê×õê).
  • thenar atrophy
    ¹«Áö?ÍÂ?¡­ê×õê)
  • toxic atrophy
    Áßµ¶¼ºÀ§Ãà(ñéÔ¸àõê×õê)
  • yellow atrophy
    Ȳ»öÀ§Ãà(¡­ê×õê)
  • anterior ischemic optic neuropathy
    Àü¹æÇãÇ÷¼º ½Ã½Å°æº´Áõ(îñÛ°úÈúìàõãÊãêÌèÜ»ñø).
  • anterior ischemic optic neuropathy
    ¾ÕÇãÇ÷½Ã½Å°æº´Áõ
  • axial optic neuritis
    Ã༺½Ã½Å°æ¿°.
  • cavity of optic cup
    ´«¼úÀܰø°£
  • choroid fissure optic fissure
    ´«¼úÀÜÆ´»õ
  • coloboma of optic disc
    ½Ã½Å°æÀ¯µÎ°á¼Õ
  • coloboma of optic nerve
    ½Ã½Å°æ°á¼Õ
  • diabetic optic neuropathy ´ç´¢
    ´ç´¢º´(¼º) ½Ã½Å°æº´Áõ.
  • evulsion of optic nerve
    ½Ã½Å°æÀûÃâ
  • excavation of optic nerve head
    ½Ã½Å°æÀ¯µÎÇÔ¸ô
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OCA oculocutaneous albinism; olivopontocerebellar atrophy; oral contraceptive agent
OPCA olivopontocerebellar atrophy
PMA index of prevalence and severity of gingivitis, where P = papillary gingiva, M = marginal gingiva, a...
PPCRA pigmented paravenous chorioretinal atrophy
PPMA progressive postmyelitis muscular atrophy
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juvenile spinal muscular atrophy Slowly progressive proximal muscular weakness and wasting, beginning in childhood, caused by degeneration of motor neurons in the anterior horns of the spinal cord; onset usually between 2 and 17 years of age; usually autosomal recessive inheritance.
Synonym: juvenile muscular atrophy, Kugelberg-Welander disease, Wohlfart-Kugelberg-Welander disease.
(05 Mar 2000)
facioscapulohumeral atrophy 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)
yellow atrophy of the liver See: acute yellow atrophy of the liver.
(05 Mar 2000)
familial spinal muscular atrophy Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised.
Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy.
(05 Mar 2000)
Kienbock's atrophy Acute atrophy of bone in an extremity following inflammation.
(05 Mar 2000)
fatty atrophy Fatty infiltration secondary to an atrophy of the essential elements of an organ or tissue.
(05 Mar 2000)
Zimmerlin's atrophy A variety of hereditary progressive muscular atrophy in which the atrophy begins in the upper half of the body.
(05 Mar 2000)
linear atrophy Bands of thin wrinkled skin, initially red but becoming purple and white, which occur commonly on the abdomen, buttocks, and thighs at puberty and/or during and following pregnancy, and result from atrophy of the dermis and overextension of the skin; also associated with ascites and Cushing's syndrome.
Synonym: atrophoderma striatum, lineae albicantes, lineae atrophicae, linear atrophy, stretch marks, stria, striae atrophicae, striate atrophy of skin, traction atrophy, vergeture.
(05 Mar 2000)
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