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"Pick's 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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  • ¿µ¹®
    ÇѱÛ
  • reticular atrophy
    ±×¹°À§Ãà, ¸Á»óÀ§Ãà
  • spinal muscular atrophy
    ô¼ö±Ù(À°)À§ÃàÁõ
  • steroid-induced atrophy
    ½ºÅ×·ÎÀ̵åÀ¯¹ßÀ§Ãà
  • subcutaneous atrophy
    ÇǺιØÀ§Ãà, ÇÇÇÏÀ§Ãà
  • senile atrophy
    ³ë³âÀ§Ãà
  • serous atrophy
    Àå¾×¼ºÀ§Ãà
  • simple atrophy
    ´Ü¼øÀ§Ãà
  • villous atrophy
    À¶¸ðÀ§Ãà
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 7 ÆäÀÌÁö: 3
  • ¿µ¹®
    ÇѱÛ
  • serous atrophy
    Àå¾×À§Ãà
  • simple atrophy
    ´Ü¼øÀ§Ãà
  • spinal muscular atrophy
    ô¼ö±ÙÀ°À§Ãà
  • steroid-induced atrophy
    ½ºÅ×·ÎÀ̵åÀ§Ãà
  • subcutaneous atrophy
    ÇÇÇÏÀ§Ãà, ÇǺιØÀ§Ãà
  • toxic atrophy
    Áßµ¶À§Ãà
  • villous atrophy
    À¶¸ðÀ§Ãà
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 6 ÆäÀÌÁö: 3
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  • progressive unilateral facial atrophy
    ÁøÇ༺ Æí¾È¸éÀ§Ãà(òäú¼àõø¸äÔØüê×õê ).
  • progressive unilateral facial atrophy
    ÁøÇ༺ Æí¾È¸éÀ§Ãà(òäú¼àõ ø¸äÔØüê×õê )
  • red atrophy
    Àû»öÀ§Ãà(îåßäê×õê)
  • renal atrophy
    ½ÅÀ§Ãà(ãìê×õê).
  • renal atrophy
    ½ÅÀ§Ãà(ãìê×õê)
  • renal atrophy
    ½ÅÀ§Ãà
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 3
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  • denervation muscular atrophy
    Å»½Å°æ¼º(÷­ãêÌèàõ) ±ÙÀ§Ãà(ÐÉê×õê).
  • dental atrophy
    Ä¡¾ÆÀ§Ãà(¡­ê×õê).
  • dentate cerebellar atrophy
    ½Å¿ÜÄ¡»óÇÙ¼Ò³úÀ§Ãà(öÍßÒú·á³Òàê×õê).
  • diffuse atrophy of alveolar bone
    ¹Ì¸¸¼º Ä¡Á¶°ñÀ§Ãà(¡­öÍðËÍéê×õê).
  • diffuse cerebral atrophy
    ¹Ì¸¸¼º ³úÀ§Ãà.
  • disuse atrophy
    ¹«¿ë¼º À§Ãà(ÙíéÄàõê×õê), ¹«À§À§Ãà, ºÎµ¿ÀÛ¼º À§Ãà.
  • disuse atrophy
    ºÒ¿ë¼º À§Ãà(ÝÕéÄàõê×õê), ¹«¿ë¼º À§Ãà(ÙíéÄàõê×õê), ¹«À§ À§Ãà, ºÎµ¿ÀÛ¼º À§Ãà.
  • eccentric atrophy
    Æí½É¼º À§Ãà(ø¶ãýàõê×õê), ¿ø½É¼º À§Ãà(¡­ê×õê).
  • eccentric atrophy
    ¿ø½É¼º À§Ãà(¡­ê×õê).
  • electric optic atrophy
    Àü±â½Ã½Å°æÀ§Ãà
  • endometrium,senile cystic atrophy
    ³ëÀμº ³¶¼º À§Ãà
  • essential iris atrophy
    º»Å¼ºÈ«Ã¤À§Ãà, Ư¹ß¼ºÈ«Ã¤À§Ãà
  • facial atrophy
    ¾È¸éÀ§Ãà
  • facioscapulohumeral atrophy
    ¾È¸é°ß°©»ó¿Ï(±Ù)À§Ãà(Áõ)(¡­Ì·Ë£ß¾èÓÐÉê×õêñø).
  • familial spinal muscular atrophy
    °¡Á·¼º ô¼ö¼º ±ÙÀ§Ãà(Áõ).
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DJOA dominant juvenile optic atrophy
DMOA diabetes mellitus-optic atrophy [syndrome]
DOA date of admission; dead on arrival; Department of Agriculture; depth of anesthesia; differential opt...
FSHSMA facioscapulohumeral spinal muscular atrophy
GA Gamblers Anonymous; gastric analysis; gastric antrum; general anesthesia; general angiography; gener...
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DRPLA Dentato-rubral and pallido-luysian atrophy
DR-PLA Dentato-rubro-pallido-luysian atrophy
GA Geographic atrophy
GA Gyrate atrophy
HCSMA Hereditary Canine Spinal Muscular Atrophy
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 3
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    ¼³¸í
  • pressure atrophy
    ¾Ð¹Ú À§Ãà
  • reticular atrophy
    ¸Á»ó À§Ãà
  • senile atrophy
    ³ë³â¼º À§Ãà, ³ëÀμº À§Ãà
    ³ªÀ̰¡ µê¿¡ µû¸¥ ¸ðµç Á¶Á÷ÀÇ »ý¸®ÀûÀÎ À§Ãà.
  • spinal progressive muscular atrophy
    ô¼ö¼º ÁøÇ༺ ±ÙÀ§ÃàÁõ
    ô¼ö ¹× ¿¬¼öÀÇ ¿îµ¿ ½Å°æ ¼¼Æ÷ÀÇ º¯¼º¿¡ ÀÇÇÏ¿© Àü½ÅÀÇ ±ÙÀ§Ãà°ú Å»·ÂÀ» ÀÏÀ¸Å°´Â º´. ¼Õ, ¹ßÀÇ ±ÙÀ° À§Ãà¿¡¼­ ½ÃÀÛÇÏ¿© Á¡Â÷·Î »óÇàÇØ¼­ ¸ñÀÇ ±ÙÀ°°ú ¸öÅëÀÇ ±ÙÀ°µµ Ä§ÇØµÈ´Ù. »ó, ÇÏÁöÀÇ ÈûÁٹݻ簡 ¾àÇØÁö°í ¹Ùºó½ºÅ° ¹Ý»ç´Â À½¼ºÀÌ µÈ´Ù. °æ°ú°¡ ±æ°í Á¶±â¿¡ »ç¸ÁÇÏ´Â ÀÏÀº ¾øÀ¸³ª, °«³­¾Æ±â¿¡¼­ º¼ ¼ö ÀÖ´Â ÀÌ º´À» º£¸£Æ®´ÏÈ÷-È£ÇÁ¸¸ º´À̶ó°í Çϸç, ¼ö³â À̳»¿¡ »ç¸ÁÇÑ´Ù. ¶Ç À̰Ͱú ±Ù¿¬°ü°è¿¡ ÀÖ´Â °¡Á·¼º ô¼ö¼º ±ÙÀ§¼º ±Ù À§ÃàÁõµµ ÀÌ º´ÀÇ ÇÑ ÇüÀÌ´Ù. 3¼¼ ÀÌÈÄÀÇ ¾î´À ¿¬·ÉÃþ¿¡¼­³ª ¹ßº´ÇÏ¸ç ±ä °æ°ú¸¦ ÃëÇÑ´Ù. Ư¼öÇÑ Ä¡·á¹ýÀº ¾ø°í ¿îµ¿ ¿ä¹ýÀÌ ÇÊ¿äÇÏ´Ù.
  • Zimmerlin's atrophy
    Áü¸Þ¸¦¸° À§Ãà
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Vulpian's atrophy Progressive spinal muscular atrophy beginning in the shoulder.
Synonym: scapulohumeral atrophy.
(05 Mar 2000)
cerebellar atrophy A degeneration of the cerebellum, particularly the Purkinje cells, as the result of abiotrophy or of toxic agents, as in alcoholism.
(05 Mar 2000)
periodontal atrophy Decrease in size and/or cellular elements of the periodontium after it has reached normal maturity.
(05 Mar 2000)
peroneal muscular atrophy A group of three familial peripheral neuromuscular disorders, sharing the common feature of marked wasting of the more distal extremities, particularly the peroneal muscle groups, resulting in "stork legs." Two of the three subtypes are hereditary sensorimotor polyneuropathies, one demyelinating in type and the other axon loss in type, while the third subgroup is an anterior horn cell disorder. It usually involves the legs before the arms; pes cavus is often the first sign; autosomal dominant, autosomal recessive, and X-linked recessive types, with severity related to genetic type.
Synonym: Charcot-Marie-Tooth disease.
(05 Mar 2000)
choroidal vascular atrophy Atrophy affecting either all choroidal vessels or only the choriocapillaris, occurring either diffusely or confined to the posterior pole of the eye.
(05 Mar 2000)
gyrate atrophy Progressive, autosomal recessive, diffuse atrophy of the choroid, pigment epithelium, and sensory retina that begins in childhood.
(12 Dec 1998)
gyrate atrophy of choroid and retina A slowly progressive atrophy of the choriocapillaris, pigmentary epithelium, and sensory retina, with irregular confluent atrophic areas and an associated ornithinuria; autosomal recessive inheritance; due to a deficiency of ornithine d-aminotransferase.
(05 Mar 2000)
Werdnig-Hoffmann 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)
compensatory atrophy Atrophy especially of an endocrine organ as a result of its function being assumed by a new source of hormone.
(05 Mar 2000)
congenital cerebellar atrophy Familial disorder that causes degeneration of various cells in the cerebellum. Two types are recognised, one in which the granular layer cells degenerate, the other in which the Purkinje cells degenerate.
(05 Mar 2000)
multiple system atrophy A name grouping together the four cerebral degenerative diseases of olivopontocerebellar atrophy, shy-drager syndrome, striatonigral degeneration, and one form of parkinson disease, considering them different forms of the same disease process.
(12 Dec 1998)
muscular atrophy Derangement in size and number of muscle fibres occurring with aging, reduction in blood supply, or following immobilization, prolonged weightlessness, malnutrition, and particularly in denervation.
(12 Dec 1998)
muscular atrophy, spinal Progressive degenerative disorder of motor neurons in the spinal cord, brainstem, and motor cortex, manifested clinically by muscular weakness, atrophy, and corticospinal tract signs in varying combinations.
(12 Dec 1998)
myopathic atrophy Muscular atrophy caused by a primary disorder of muscle.
(05 Mar 2000)
postmenopausal atrophy Atrophy following menopause, as of the genital organs.
(05 Mar 2000)
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