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"central areolar choroidal 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.
´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 3
  • ¿µ¹®
    ÇѱÛ
  • macular atrophy
    1. ÇǺιÝÁ¡À§Ãà(Áõ) 2. Ȳ¹ÝÀ§Ãà
  • neurogenic muscular atrophy
    ½Å°æ¼º±Ù(À°)À§Ãà
  • olivopontocerebellar atrophy
    ¿Ã¸®ºê´Ù¸®³ú¼Ò³úÀ§Ãà
  • optic atrophy
    ½Ã(°¢)½Å°æÀ§Ãà
  • optic nerve atrophy
    ½Ã(°¢)½Å°æÀ§Ãà
  • pigmentary atrophy
    »ö¼Ò¼ºÀ§Ãà
  • pressure atrophy
    ¾Ð¹ÚÀ§Ãà
  • progressive spinal muscular atrophy
    ÁøÇàô¼ö¼º±Ù(À°)À§ÃàÁõ
  • perifollicular macular atrophy
    ÅÐÁýÁÖÀ§¹ÝÁ¡À§Ãà
  • peripapillary chorioretinal atrophy
    À¯µÎÁÖÀ§¸Æ¶ô¸Á¸·À§Ãà
  • 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
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 3
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    ÇѱÛ
  • myopathic atrophy
    ±ÙÀ°º´ÁõÀ§Ãà
  • neural progressive muscular atrophy
    ½Å°æÁøÇà±ÙÀ°À§Ãà
  • neurogenic muscular atrophy
    ½Å°æÅ¿±ÙÀ°À§Ãà
  • neurospinal muscular atrophy
    ½Å°æÃ´¼ö±ÙÀ°À§Ãà
  • olivopontocerebellar atrophy
    ¿Ã¸®ºê´Ù¸®¼Ò³úÀ§Ãà
  • optic atrophy
    ½Ã°¢½Å°æÀ§Ãà
  • perifollicular macular atrophy
    ÅÐÁýÁÖÀ§¹ÝÁ¡À§Ãà
  • peripapillary chorioretinal atrophy
    À¯µÎÁÖÀ§¸Æ¶ô¸Á¸·À§Ãà
  • pigmentary atrophy
    »ö¼Ò¼ºÀ§Ãà
  • pressure atrophy
    ¾Ð¹ÚÀ§Ãà
  • reticular atrophy
    ¸Á»óÀ§Ãà
  • senile atrophy
    ³ë³âÀ§Ãà
  • serous atrophy
    Àå¾×À§Ãà
  • simple atrophy
    ´Ü¼øÀ§Ãà
  • spinal muscular atrophy
    ô¼ö±ÙÀ°À§Ãà
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 3
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    ÇѱÛ
  • hemilingual atrophy
    ÆíÃø¼³À§Ãà
  • hereditary optic atrophy
    À¯Àü¼º½Ã½Å°æÀ§Ãà.
  • hereditary optic atrophy
    À¯Àü¼º ½Ã½Å°æÀ§Ãà.
  • hypothenar atrophy
    ¼ÒÁö±¸À§Ãà.
  • hypothenar atrophy
    ¼ÒÁö±¸ À§Ãà(á³ò¦Ï¹êÍõê).
  • infantile muscular atrophy =Werdnig-Hoffmann disease
    ¿µ¾ÆÇü±ÙÀ§ÃàÁõ(?ä®û¡ÐÉê×õêñø).
  • infantile muscular atrophy =Werdnig-Hoffmann disease
    ¿µ¾ÆÇü ±ÙÀ§ÃàÁõ(?ä®û¡ÐÉê×õêñø).
  • infantile progressive spinal muscular atrophy
    ¿µ¾ÆÁøÇ༺ ô¼ö¼º ±ÙÀ§Ãà(Áõ).
  • peroneal muscular atrophy
    ºñ°ñ±Ù À§ÃàÁõ(ÝëÍéÐÉê×õêñø).
  • pigmentary atrophy
    »ö¼Ò¼º À§Ãà(ßäáÈàõ ê×õê)
  • postinflammatory optic atrophy
    ¿°ÁõÈĽýŰæÀ§Ãà
  • postneuritic optic atrophy
    ¿°ÁõÈĽýŰæÀ§Ãà
  • pressure atrophy
    ¾Ð¹ÚÀ§Ãà(äâÚÞê×õê).
  • primary optic atrophy
    ¿ø¹ß½Ã½Å°æÀ§Ãà(ê«Û¡ãÊãêÌèê×õê).
  • primary optic atrophy
    ¿ø¹ß(¼º) ½Ã½Å°æÀ§Ãà(ê«Û¡(àõ) ãÊãêÌèê×õê)
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 3
  • ¿µ¹®
    ÇѱÛ
  • choroidal sclerosis
    ¸Æ¶ô¸·°æÈ­(Áõ)
  • inferior choroidal vein
    ¾Æ·¡¸Æ¶ôÁ¤¸Æ
  • lateral posterior choroidal branches
    °¡Âʵڸƶô°¡Áö
  • lateral ventricular choroidal branches
    °¡Âʳú½Ç¸Æ¶ô°¡Áö
  • medial posterior choroidal branches
    ¾ÈÂʵڸƶô°¡Áö
  • superior choroidal vein
    À§¸Æ¶ôÁ¤¸Æ
  • third ventricular choroidal branches
    ¼Â°³ú½Ç¸Æ¶ô°¡Áö
  • acute yellow atrophy
    ±Þ¼º Ȳ»öÀ§Ãà(Áõ)(ÐáàõüÜßäê×õêñø) °£(ÊÜ)
  • acute yellow atrophy
    ±Þ¼º Ȳ»öÀ§Ãà(Áõ)(ÐáàõüÜßäê×õêñø) °£(ÊÜ)ÀÇ .
  • alveolar atrophy<³ª> atrophia alveolaris
    Ä¡Á¶À§Ãà(öÍðËê×õê).
  • atrophy
    ˤ̈
  • atrophy from disuse =disuse a.
    ºñȰµ¿(¼º)À§Ãà, ¹«À§(ÙíêÓ)À§Ãà.
  • atrophy noir
    Èæ»öÀ§Ãà
  • atrophy, brown
    À§Ãà(¡­), °¥»ö
  • atrophy<³ª> atrophia, ºÒ atrophie
    À§Ãà(Áõ)(ê×õêñø), ¹«¿µ¾çÁõ(Ùíç½å×ñø)
´ëÇÑÇØºÎÇÐȸ ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 3
  • ¿µ¹®
    ÇѱÛ
  • Central tendon
    Á߽ɳÎÈûÁÙ
    [¿¾ ¿ë¾î] °ÇÁß½É
  • Central tegmental tract
    Áß½ÉµÚÆÇ·Î
    [¿¾ ¿ë¾î] Áß½ÉÇǰ³·Î
  • Central lacteal
    Á߽ɸ²ÇÁ°ü
    [¿¾ ¿ë¾î] Áß½ÉÀӯİü
  • Central lymph nodes
    Á߽ɸ²ÇÁÀý
    [¿¾ ¿ë¾î] Áß½ÉÀÓÆÄÀý
  • Central heterochromatic part
    Á߽ɹ¶Ä£¿°»öÁúºÎºÐ
    [¿¾ ¿ë¾î] Áß½ÉÀÌ¿°»öÁúºÎ
  • Central microtubule
    Á߽ɹ̼¼°ü
    [¿¾ ¿ë¾î] Á߽ɹ̼Ұü
  • Central part
    Á߽ɺκÐ
    [¿¾ ¿ë¾î] Á߽ɺÎ
  • Central attachment
    Á߽ɺÎÂø
    [¿¾ ¿ë¾î] Á߽ɺÎÂø
  • Central insertion
    Á߽ɺÎÂø
    [¿¾ ¿ë¾î] Á߽ɺÎÂø
  • Central fiber
    Á߽ɼ¶À¯
    [¿¾ ¿ë¾î] Á߽ɼ¶À¯
  • Central lobule
    Á߽ɼҿ±
    [¿¾ ¿ë¾î] ¼Ò³úÁ߽ɼҿ±
  • Ala of central lobule
    Á߽ɼҿ±³¯°³
    [¿¾ ¿ë¾î] Á߽ɼҿ±ÀÍ
  • Central thalamic radiations
    Á߽ɽûóºÎê»ì
    [¿¾ ¿ë¾î] ±Ã½É½Ã»ó¹æ»ç
  • Central thalamic radiations
    Á߽ɽûóºÎê»ì
    [¿¾ ¿ë¾î] Áß½É½Ã»ó¹æ»ç
  • Central gelatinous substance
    Á߽ɾƱ³Áú
    [¿¾ ¿ë¾î] Á߽ɱ³¾çÁú
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 3
CSMA chronic spinal muscular atrophy
DIDMOA diabetes insipidus-diabetes mellitus-optic atrophy [syndrome]
DIDMOAD diabetis insipidus, diabetes mellitus, otpic atrophy, deafness [syndrome]
DIMOAD diabetes insipidus, diabetes mellitus, optic atrophy, deafness
DJOA dominant juvenile optic atrophy
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 3
GA Geographic atrophy
GA Gyrate atrophy
HCSMA Hereditary Canine Spinal Muscular Atrophy
HA Hippocampal atrophy
MSA Multiple System Atrophy
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 3
  • ¿µ¹®
    ÇѱÛ
    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
  • central
    Áß½ÉÀÇ, Áß¾ÓÀÇ, ÁßÃßÀÇ, ÁßÃß¼ºÀÇ, ÁßÃß¼º, Á߽ɼº
  • central action
    ÁßÃß ÀÛ¿ë
  • central amaurosis
    ÁßÃß¼º Èæ¾Ï½Ã
  • central anesthesia
    Á߽ɼº ¹«°¨°¢Áõ
    ½Å°æ ÀÓÆÞ½ºÀÇ ÁßÃß¼º Â÷´Ü°ú ÁßÃ߽ŰæÀÇ ÁúȯÀ¸·Î ÀÎÇÑ ¹«°¨°¢Áõ.
  • central aphasia
    ÁßÃß¼º ½Ç¾îÁõ
  • central artery cerebri mediae
    ÁߺΠ³úµ¿¸Æ Áß½ÉÁö
  • central artery of retina
    ¸Á¸· Á᫐ µ¿¸Æ
  • central attachment
    Á᫐ ºÎÂø
  • central bearing
    Á᫐ ÁöÁö
  • central bearing point
    Á᫐ ÁöÁöÁ¡
    Áß¾Ó ÁöÁö ÀåÄ¡ÀÇ Á¢ÃËÁ¡.
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 3
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)
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)
Pick's atrophy Circumscribed atrophy of the cerebral cortex.
Synonym: lobar sclerosis, progressive circumscribed cerebral atrophy.
(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)
cyanotic atrophy Atrophy due to destruction of the parenchymatous cells of an organ as a consequence of chronic venous congestion.
Synonym: red atrophy.
(05 Mar 2000)
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