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"Hereditary ataxia, unspecified"¿¡ ´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
  • hereditary coagulation disorder
    À¯ÀüÀÀ°íÀå¾Ö
  • hereditary coproporphyria
    À¯ÀüÄÚÇÁ·ÎÆ÷¸£ÇǸ°Áõ
  • hereditary disease
    À¯Àüº´
  • hereditary disorder
    À¯ÀüÀå¾Ö, À¯ÀüÁúȯ
  • hereditary epilepsy
    À¯Àü°£Áú
  • hereditary hearing impairment
    À¯Àüû·ÂÀå¾Ö
  • hereditary hemorrhagic telangiectasia
    À¯Àü¼ºÃâÇ÷¸ð¼¼Ç÷°üÈ®ÀåÁõ
  • hereditary leptocytosis
    À¯ÀüÇ¥ÀûÀûÇ÷±¸Áõ
  • hereditary lymphedema
    À¯Àü¸²ÇÁºÎÁ¾
  • hereditary methemoglobinemic cyanosis
    À¯Àü¸ÞÆ®Çì¸ð±Û·ÎºóÇ÷û»öÁõ
  • hereditary motor sensory neuropathy
    À¯Àü¿îµ¿°¨°¢½Å°æº´(Áõ)
  • hereditary multiple exostosis
    À¯Àü´Ù¹ß»Àµ¹ÃâÁõ, À¯Àü´Ù¹ß¿Ü°ñÁõ
  • hereditary mutilating keratoma
    À¯ÀüÀý´Ü°¢È­Á¾
  • hereditary nonpolyposis colorectal cancer
    1. À¯Àü¼ººñÆú¸³À߷ϰðâÀÚ¾Ï 2. À¯Àü¼ººñÆú¸³´ëÀå¾Ï
  • hereditary opalescent dentine
    À¯ÀüÁ¥ºû»ó¾ÆÁú
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    ÇѱÛ
  • hereditary benign intraepithelial dyskeratosis
    À¯Àü¾ç¼º»óÇdz»ÀÌ»ó°¢È­Áõ
  • hereditary coagulation disorder
    À¯ÀüÀÀ°íÀå¾Ö
  • hereditary opalescent dentine
    À¯ÀüÀ¯¹é»ö»ó¾ÆÁú
  • recessive hereditary disease
    ¿­¼ºÀ¯Àüº´
  • hereditary epilepsy
    À¯Àü°£Áú
  • hereditary bullous epidermolysis
    À¯Àü¹°ÁýÇ¥Çǹڸ®Áõ
  • hereditary multiple exostosis
    À¯Àü´Ù¹ß»Àµ¹ÃâÁõ
  • hereditary
    À¯Àü-
  • hereditary leptocytosis
    À¯ÀüÇ¥ÀûÀûÇ÷±¸Áõ
  • hereditary lymphedema
    À¯Àü¸²ÇÁºÎÁ¾
  • hereditary spherocytosis
    À¯ÀüµÕ±ÙÀûÇ÷±¸Áõ, À¯Àü±¸ÇüÀûÇ÷±¸Áõ
  • hereditary stigma
    À¯Àü¡ǥ
  • hereditary syphilis
    (¢¡congenital syphilis) ¼±Ãµ¸Åµ¶
  • hereditary trait
    À¯Àü¼ÒÁú
  • hereditary tremor
    (¢¡essential tremor) º»Å¶³¸², À¯Àü¶³¸², ¿øÀθ𸦶³¸²
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
  • hereditary benign intraepithelial dyskeratosis
    À¯Àü¼º ¾ç¼º »óÇdz» ÀÌ»ó°¢È­Áõ
  • hereditary brown enamel
    À¯Àü¼º °¥»ö ¹ý³¶Áú.
  • hereditary brown tooth
    À¯Àü¼º °¥»öÄ¡¾Æ.
  • hereditary bullous epidermolysis ³ª e.bullosa hereditaria
    À¯Àü¼º Ç¥ÇǼöÆ÷Áõ.
  • hereditary cerebellar sclerosis
    À¯Àü¼º ¼Ò³ú°æÈ­Áõ.
  • hereditary cerebral hemorrhages with amyloidosis(hchwa)
    À¯Àü¼º ³úÃâÇ÷, ¾Æ¹Ð·ÎÀ̵åÁõ¼º
  • hereditary chorea
    À¯Àü(¼º) ¹«µµº´.
  • hereditary coagulation disorder
    À¯Àü¼º ÀÀ °íÀå¾Ö.
  • hereditary coproporphyria
    À¯Àü¼º ÄÚÇÁ·ÎÆ÷ ¸£ÇǸ®¾Æ.
  • hereditary corneal dystrophy
    À¯Àü¼º°¢¸·ÀÌ¿µ¾çÁõ.
  • hereditary corneal dystrophy
    À¯Àü¼º °¢¸·ÀÌ ¿µ¾çÁõ.
  • hereditary craniofacial dysostosis
    À¯Àü¼º µÎ°³¾È¸éÀ̰ñÁõ(¡­ÔéËÏäÔØüì¶Íéñø).
  • hereditary craniofacial dysostosis
    À¯Àü¼º µÎ°³¾È¸éÀ̰ñÁõ
  • hereditary deaf-mutism
    À¯Àü¼º ³ó¾Æ
  • hereditary deafmutism
    À¯Àü¼º ³ó¾Æ (¡­Öìä¯).
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  • ¿µ¹®
    ÇѱÛ
  • cerebellar ataxia
    ¼Ò³ú¼º ¿îµ¿½ÇÁ¶(Áõ).
  • congenital cerebellar ataxia
    ¼±Ãµ¼º ¼Ò³ú¼º (¿îµ¿)½ÇÁ¶(¡­á³Òààõê¡ÔÑã÷ðà).
  • cordis ataxia =fibrillation
    ¼¼µ¿(á¬ÔÑ).
  • cortical ataxia
    ÇÇÁú(¼º)¿îµ¿ºÒ´É(Áõ)(ù«òõàõê¡ÔÑÝÕÒöñø).
  • cortical ataxia
    ÇÇÁú¼º (¿îµ¿)½ÇÁ¶(Áõ)(¡­ê¡ÔÑã÷ðàñø).
  • diphtheritic ataxia
    µðÇÁÅ׸®¾Æ¼º ¿îµ¿½ÇÁ¶(¡­ê¡ÔÑã÷ðà).
  • dynamic ataxia =locomotive a.
    ¿ªµ¿Àû ¿îµ¿½ÇÁ¶(æ³ÔÑîÜê¡ÔÑã÷ðà).
  • friedreichs ataxia
    ÇÁ¸®À̵å¶óÀÌÈ÷ ¿îµ¿½ÇÁ¶(Áõ)
  • frontal ataxia
    ÀüµÎ¿±¼º ¿îµ¿½ÇÁ¶(Áõ).
  • frontal lobe ataxia
    ÀüµÎ¿±¼º ¿îµ¿½ÇÁ¶.
  • hysterical ataxia
    È÷½ºÅ׸®¼º ¿îµ¿½ÇÁ¶
  • hysterical ataxia
    È÷½ºÅ׸®¼º ¿îµ¿½ÇÁ¶.
  • juvenile ataxia
    ¿¬¼Ò¼º ¿îµ¿½ÇÁ¶(Áõ).
  • kinetic ataxia
    ¿îµ¿¼º ½ÇÇàÁõ(¡­ã÷ú¼ñø).
  • labyrinthic ataxia
    ¹Ì·Î¼º ¿îµ¿½ÇÁ¶(¡­ê¡ÔÑ ã÷ðà).
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 2
AEMK ataxia episodica with myokymia
AMC academic medical center; acetylmethyl carbinol; Animal Medical Center; antibody-mediated cytotoxicit...
AREPA acetazolamide-responsive familial paroxysmal ataxia
ARSACS autosomal recessive spastic ataxia of Charlevoix-Saguenay
AT abdominal thrusts; achievement test; Achilles tendon; Achard-Thiers [syndrome]; adaptive thermogenes...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 2
SCA1 Spinocerebellar Ataxia 1
SCA2 Spinocerebellar Ataxia Type 2
SCA Spinocerebellar ataxia
SCA-2 Spinocerebellar ataxia 2
SCA7 Spinocerebellar ataxia 7
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 14 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • hereditary craniofacial dysostosis
    À¯Àü¼º µÎ°³ ¾È¸é À̰ñÁõ
    ž»ó µÎ°³, ¾È±¸ µ¹Ãâ, ¾ç¾È °Ý¸®, »ç½Ã, ¾Þ¹«»õ ºÎ¸® ¸ð¾ç1114-377786/377786Àüµ¹À» ¼ö¹ÝÇÏ´Â »ó¾Ç Çü¼º ºÎÀüÀ» Ư¡À¸·Î ÇÏ´Â À¯ÀüÀû Áúȯ.
  • hereditary disease
    À¯Àüº´
    À¯ÀüÀÚ¿¡ ÀÇÇÏ¿© ÀϾ´Â ½ÅüÀû, Á¤½ÅÀûÀÎ ÀÌ»óÀÇ ÃÑĪ. À¯Àü¼º ÁúȯÀ̶ó°íµµ ÇÑ´Ù. º´, ÀÌ»ó ÇüÁúÀÌ À¯ÀüÀû ¿äÀΰú °ü·ÃÀÌ ÀÖÀ½¿¡ µû¶ó¼­ ¹Ýµå½Ã À¯ÀüÀÚ¿¡ ÀÇÇÏÁö ¾Ê´Â À¯ÀüÀûÀÎ º´µµ À¯Àüº´À̶ó°í ÇÏ°Ô µÇ¾ú´Ù. 1°³ÀÇ ¿ì¼º À¯ÀüÀÚ¿¡ ÀÇÇÏ¿© ÀϾ´Â ÇåÆÃÅÏ ¹«µµº´, ¹ß·»ºÎ¸£Å© ÁõÈıº, ¿­¼º À¯ÀüÀÚÀÇ µ¿Çü Á¢ÇÕ¿¡ ÀÇÇÏ¿© ³ªÅ¸³ª´Â ¹éÀÚ, Æä´ÒÄÉÅæ´¢Áõ, X ¿°»öü À§ÀÇ ¹Ý¼º À¯ÀüÀÚ¿¡ ÀÇÇÑ Àû·Ï »ö¸Í, Ç÷¿ìº´, ÁøÇ༺ ±Ù µð½ºÆ®·ÎÇÇÁõ µîÀº ¸í¹éÈ÷ ÀÌÀ¯ ÀüÀÚ¿¡ ÀÇÇÑ °ÍÀ¸·Î¼­, À¯Àüº´ÀÇ ´ëÇ¥ÀûÀÎ °ÍÀ̶ó°í ÇÒ ¼ö ÀÖ´Ù. ¹Ý¼º À¯ÀüÀÚ´Â X ¿°»öü À§¿¡ À§Ä¡ÇÏ´Â °Í¸¸ ¾Ë·ÁÁ® ÀÖ°í, ³²¼ºÀ» °áÁ¤ÇÏ´Â Y ¿°»öü À§¿¡´Â ÇöÀç±îÁö ƯÈ÷ È®½ÇÇÑ ÇüÁúÀ» °áÁ¤ÇÏ´Â À¯ÀüÀÚ´Â Á¸ÀçÇÏÁö ¾Ê´Â´Ù°í º¸°í ÀÖ´Ù. À¯ÀüÀÚ¿¡ ÀÇÇÑ ÀÌ»óÀ̳ª º´Àº Ãâ»ýÇÏ´Â ¾Æ±âÀÇ 1 %°¡ ÀÌ¹Ì °¡Áö°í Àְųª ¹ßº´ÇÒ °¡´É¼ºÀ» Áö´Ï°í ÀÖ´Ù. ¿°»öüÀÇ ±¸Á¶ ¶Ç´Â ±¸¼ºÀÇ ÀÌ»ó¿¡ ÀÇÇÏ¿© ÀϾ´Â ¿©·¯ °¡Áö ÀÌ»ó ´Ù¿î ÁõÈıº, ÅÍ³Ê ÁõÈıº, Ŭ¶óÀÎÆçÅÍ ÁõÈıº µîµµ ¿°»öü À§¿¡ À¯ÀüÀÚ°¡ ÀÖ´Ù°í ÇÏ´Â Àǹ̿¡¼­´Â À¯ÀüÇÐÀûÀÎ °ÍÀ̶ó°í ÇÒ ¼ö ÀÖ´Ù. ±×·¯³ª ´ë°³´Â ÀÌ»ó °³Ã¼¸¦ ¸¸µç ¹è¿ìÀÚ
  • hereditary disturbance
    À¯Àü¼º Àå¾Ö
    ¼±ÃµÀûÀ¸·Î ¾î¹öÀ̷κÎÅÍ ÀÚ¼Õ¿¡°Ô ¹°·ÁÁ® ³»¸®´Â Áúº´.
  • hereditary ectodermal dysplasia
    À¯Àü¼º ¿Ü¹è¿±¼º ÀÌÇü¼ºÁõ
  • hereditary enamel hypoplasia
    À¯Àü¼º ¹ý¶ûÁú ÀúÇü¼ºÁõ
    Ä¡¾Æ ¹ý¶ûÁúÀÇ À¯ÀüÀû ºÒ¿ÏÀü Çü¼º ¶Ç´Â ¹ßÀ° ÀÌ»ó.
  • hereditary erythropoietic porphyria
    À¯Àü¼º ÀûÇ÷±¸ Á¶Ç÷¼º Æ÷¸£ÇǸ°Áõ
  • hereditary gingival fibromatosis
    À¯Àü¼º Ä¡Àº ¼¶À¯Á¾Áõ
    ÀüüÀûÀÎ Ä¡ÀºÀÇ °úÀ× Áõ½ÄÀ¸·Î ¿µ±¸ÀüÄ¡ ¸ÍÃ⠽ñ⿡ ³ªÅ¸³­´Ù. À¯Àü ¶Ç´Â ºñÀ¯ÀüÀÇ °æ¿ìµµ ¸¹´Ù. »ó¿°»öü ¿ì¼ºÀ¯ÀüÀ» ÇÏ´Â °æ¿ì°¡ ¸¹´Ù. Ä¡ÀºÀÌ Àüü ¾Ç°ñÀ̳ª ÇÑÂÊ ¾Ç°ñ¿¡ ±¹ÇÑµÇ¾î ¼¶À¯¼º ºñ´ë¸¦ º¸ÀδÙ. ¾î¸°ÀÌ¿¡°Ô È£¹ßÇϸç Ä¡¾ÆÀÇ ¸ÍÃâÀ» ¹æÇØÇÏ´Â °æ¿ì°¡ ¸¹´Ù.
  • hereditary ichthyoacanthotoxin
    À¯Àü¼º ¾î¸° ±Ø¼¼Æ÷ µ¶¼Ò
  • hereditary nature
    À¯Àü¼º
  • hereditary opalescent dentin
    À¯Àü¼º À¯¹é»ö »ó¾ÆÁú
    »ó¾ÆÁú Çü¼º ºÎÀüÁõ¿¡ ³ªÅ¸³ª´Â À¯¹é±¤À» ¹ß»êÇÏ´Â °Í °°ÀÌ º¸ÀÌ´Â °¥»öÀÇ »ó¾ÆÁú.
  • hereditary porphyria cutanea tarda
    À¯Àü¼º ¸¸¹ß¼º ÇǺΠÆ÷¸£ÇǸ°Áõ
  • hereditary syphilis
    ¼±Ãµ ¸Åµ¶
    µ¿ÀǾî=congenital sy
  • hereditary telangiectasia
    À¯Àü¼º ¸ð¼¼Ç÷°ü È®ÀåÁõ
    ¼±ÃµÀûÀ¸·Î ¸ð¼¼Ç÷°üÀÌ È®ÀåµÇ´Â ÁúȯÀ¸·Î °üÂû ½Ã ¹ÝÁ¡»ó È«¹ÝÀ¸·Î ³ªÅ¸³ª°í °³º°ÀûÀ¸·Î È®ÀåµÈ Ç÷°ü ¾ç»óÀ» °üÂûÇÒ ¼ö ÀÖ´Ù.
  • lebers hereditary optic neuropathy
    ·¹¹ö¾¾ ¼±Ãµ¼º ½Ã½Å°æº´Áõ
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
vestibulocerebellar ataxia Ataxia due to disease of the central vestibular system or its cerebellar components, manifested clinically by an unsteady gait, nystagmus, and incoordination of arm and leg movements.
(05 Mar 2000)
respiratory ataxia Completely irregular breathing pattern, with continually variable rate and depth of breathing; results from lesions in the respiratory centres in the brainstem, extending from the dorsomedial medulla caudally to the obex.
Synonym: ataxic breathing, Biot's breathing, respiratory ataxia.
(05 Mar 2000)
cerebellar ataxia Loss of muscle coordination caused by disorders of the cerebellum.
(05 Mar 2000)
chronic ataxia Persistent ataxia, most often caused by hereditary cerebellar or metabolic disorders.
(05 Mar 2000)
moral ataxia Inconstancy of ideas and of conscious intent, as a manifestation of hysteria.
(05 Mar 2000)
motor ataxia Ataxia developing upon attempting to perform coordinated muscular movements.
Synonym: kinetic ataxia.
(05 Mar 2000)
sensory ataxia An ataxia due to impairment of position sense caused by lesions located at some point along the central or peripheral sensory pathways.
(05 Mar 2000)
hysterical ataxia Weakening of the muscle sense and increased sensibility of the skin, in hysteria.
Synonym: hysterical ataxia.
(05 Mar 2000)
spinal ataxia Ataxia due to spinal cord disease, as in tabes dorsalis.
(05 Mar 2000)
spinocerebellar ataxia The most common hereditary ataxia, with onset in middle to late childhood, manifested as limb ataxia, nystagmus, kyphoscoliosis, and pes cavus; the major pathological changes are found in the posterior columns of the spinal cord; most often autosomal recessive inheritance.
(05 Mar 2000)
static ataxia Inability to preserve equilibrium while standing, due to loss of myesthesia; present during the resting state.
(05 Mar 2000)
optic ataxia An inability to guide the hand toward an object using visual information; seen in Balint's syndrome.
(05 Mar 2000)
enzootic ataxia A metabolic disease of lambs characterised clinically by progressive incoordination of the hind limbs and pathologically by disruption of neuron and myelin development in the central nervous system; caused by a deficiency of metabolizable copper in the ewe during the last half of her pregnancy.
Synonym: swayback.
(05 Mar 2000)
equine spinal ataxia A disease of young horses characterised by progressive weakness and incoordination, most evident in the hind legs; it is associated with lesions in the cervical region of the spinal cord and is the result of compression of the spinal cord by malformed cervical vertebrae.
(05 Mar 2000)
kinetic ataxia Ataxia developing upon attempting to perform coordinated muscular movements.
Synonym: kinetic ataxia.
(05 Mar 2000)
ÀÌ ¾Æ·¡ ºÎÅÍ´Â °á°ú°¡ ¾ø½À´Ï´Ù.
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