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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 ataxia
    À¯Àü½ÇÁ¶
  • hereditary cerebellar ataxia
    À¯Àü¼Ò³ú½ÇÁ¶
  • ataxia
    ½ÇÁ¶
  • ataxia telangiectasia
    ¸ð¼¼°üÈ®Àå½ÇÁ¶
  • bulbar ataxia
    ¼û³ú½ÇÁ¶
  • central ataxia
    ÁßÃß½ÇÁ¶
  • cerebellar ataxia
    ¼Ò³ú½ÇÁ¶
  • gluten ataxia
    ±Û·çÅÙ½ÇÁ¶
  • hysterical ataxia
    È÷½ºÅ׸®½ÇÁ¶
  • locomotor ataxia
    À̵¿½ÇÁ¶
  • sensory ataxia
    °¨°¢¼º½ÇÁ¶
  • congenital hereditary hearing loss
    ¼±ÃµÀ¯Àü³­Ã»
  • hereditary
    À¯Àü-
  • hereditary benign intraepithelial dyskeratosis
    À¯Àü¾ç¼º»óÇdz»ÀÌ»ó°¢È­Áõ
  • hereditary chorea
    À¯Àü¹«µµº´
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  • ¿µ¹®
    ÇѱÛ
  • hereditary
    À¯Àü-
  • hereditary motor sensory neuropathy
    À¯Àü¿îµ¿°¨°¢½Å°æº´Áõ
  • hereditary spherocytosis
    À¯ÀüµÕ±ÙÀûÇ÷±¸Áõ, À¯Àü±¸ÇüÀûÇ÷±¸Áõ
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  • ¿µ¹®
    ÇѱÛ
  • hereditary ataxia
    À¯ÀüÁ¶È­¿îµ¿ºÒ´É
  • ataxia
    Á¶È­¿îµ¿¸øÇÔÁõ, Á¶È­¿îµ¿ºÒ´É
  • ataxia telangiectasia
    ¸ð¼¼Ç÷°üÈ®À强Á¶È­¿îµ¿ºÒ´É
  • bulbar ataxia
    ¼û³úÁ¶È­¿îµ¿ºÒ´É
  • central ataxia
    ÁßÃßÁ¶È­¿îµ¿ºÒ´É
  • cerebellar ataxia
    ¼Ò³úÁ¶È­¿îµ¿ºÒ´É
  • hysterical ataxia
    È÷½ºÅ׸®Á¶È­¿îµ¿ºÒ´É
  • locomotor ataxia
    (¢¡tabes dorsalis) ô¼ö¸Åµ¶, ô¼ö·Î
  • sensory ataxia
    °¨°¢¼ºÁ¶È­¿îµ¿ºÒ´É
  • congenital hereditary hearing loss
    ¼±ÃµÀ¯Àü³­Ã»
  • hereditary chorea
    À¯Àü¹«µµº´
  • hereditary coproporphyria
    À¯ÀüÄÚÇÁ·ÎÆ÷¸£ÇǸ°Áõ
  • hereditary methemoglobinemic cyanosis
    À¯Àü¸ÞÆ®Çì¸ð±Û·ÎºóÇ÷û»öÁõ
  • hereditary disease
    À¯Àüº´
  • hereditary disorder
    À¯ÀüÀå¾Ö, À¯ÀüÁúȯ
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  • ¿µ¹®
    ÇѱÛ
  • hereditary ataxia
    À¯Àü(¼º) ¿îµ¿½ÇÁ¶.
  • hereditary cerebellar ataxia
    À¯Àü¼º ¼Ò³ú¼º ¿îµ¿½ÇÁ¶.
  • hereditary spinal ataxia
    À¯Àü¼º ô¼ö¿îµ¿½ÇÁ¶(¡­ô±âÐê¡ÔÑã÷ðà).
  • Friedreich s ataxia
    ÇÁ¸®À̵å¶óÀÌÈ÷ ¿îµ¿½ÇÁ¶(Áõ).
  • acute ataxia
    ±Þ¼º ¿îµ¿½ÇÁ¶(¡­ê¡ÔÑã÷ðà).
  • friedreichs ataxia
    ÇÁ¸®À̵å¶óÀÌÈ÷ ¿îµ¿½ÇÁ¶(Áõ)
  • hysterical ataxia
    È÷½ºÅ׸®¼º ¿îµ¿½ÇÁ¶.
  • hysterical ataxia
    È÷½ºÅ׸®¼º ¿îµ¿½ÇÁ¶
  • Hereditary camptodactyly
    À¯Àü¼º ±¼ÁöÁõ
  • hearing loss, congenital hereditary
    ¼±Ãµ(¼º) À¯Àü¼º ³­Ã»
  • hereditary
    À¯Àü¼ºÀÇ
  • hereditary adrenogenital syndrome
    À¯Àü¼º ºÎ½Å¼º±â¼º ÁõÈıº.
  • hereditary angioedema
    À¯Àü¼º ¸Æ°üºÎÁ¾
  • hereditary angioedema
    À¯Àü¼ºÇ÷°üºÎÁ¾
  • hereditary aphasia
    À¯Àü(¼º) ½Ç¾î(Áõ).
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  • ¿µ¹®
    ÇѱÛ
  • hereditary ataxia
    À¯Àü(¼º) ¿îµ¿½ÇÁ¶.
  • hereditary cerebellar ataxia
    À¯Àü¼º ¼Ò³ú¼º ¿îµ¿½ÇÁ¶.
  • hereditary spinal ataxia
    À¯Àü¼º ô¼ö¿îµ¿½ÇÁ¶(¡­ô±âÐê¡ÔÑã÷ðà).
  • acute ataxia
    ±Þ¼º ¿îµ¿½ÇÁ¶(¡­ê¡ÔÑã÷ðà).
  • articulative ataxia
    °üÀýÇü ½ÇÁ¶
  • ataxia
    ¿îµ¿½ÇÁ¶(ê¡ÔÑã÷ðà)
  • ataxia telangiectasia
    Ç÷°üÈ®À强 ¿îµ¿½ÇÁ¶Áõ.
  • ataxia telangiectasia
    ¸ð¼¼Ç÷°üÈ®À强(Ç÷°üÈ®À强) ¿îµ¿½ÇÁ¶Áõ(Ù½á¬úìηüªíåàõê¡ÔÑã÷ðàñø)
  • ataxia tremor
    ¿îµ¿½ÇÁ¶¼º ÁøÀü.
  • ataxia-telangiectasia
    Ç÷°üÈ®À强 ¿îµ¿½ÇÁ¶Áõ
  • ataxia-telangiectasia
    ¸ð¼¼Ç÷°üÈ®À强¿îµ¿½ÇÁ¶
  • ataxia<³ª> ataxy
    ¿îµ¿½ÇÁ¶(ê¡ÔÑã÷ðà), ½ÇÁ¶(ã÷ðà).
  • autonomic ataxia
    ÀÚÀ²½Å°æ¼º ¿îµ¿½ÇÁ¶.
  • bulbar ataxia
    ¿¬¼ö¼º ¿îµ¿½ÇÁ¶(¡­ê¡ÔÑã÷ðà).
  • central ataxia
    ÁßÃß¼º ¿îµ¿½ÇÁ¶Áõ(¡­ê¡ÔÑã÷ðàñø).
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  • ¿µ¹®
    ÇѱÛ
  • hereditary code
    À¯Àü ºÎÈ£(ë¶îîݬûÜ)
  • hereditary material
    À¯Àü ¹°Áú(ë¶îîÚªòõ)
KI ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 7 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • ataxia
    ¿îµ¿½ÇÁ¶, ½ÇÁ¶
  • vestibular ataxia
    ÀüÁ¤¼º¿îµ¿½ÇÁ¶
  • hereditary
    À¯Àü¼ºÀÇ
  • hereditary craniofacial dysostosis
    À¯Àü¼ºµÎ°³¾È¸éÀ̰ñÁõ
  • hereditary disease
    À¯Àüº´
  • hereditary ectodermal polydysplasia
    À¯Àü¼º¿Ü¹è¿±¼º´Ù¹ßÀÌÇü¼ºÁõ
  • hereditary hemorrhagic telangiectasia
    À¯Àü¼ºÃâÇ÷¼º¸ð¼¼Ç÷°üÈ®Àå
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
STANDOUT soft thresholding and depth cueing of unspecified techniques
URD unspecified respiratory disease; upper respiratory disease
ACA abnormal coronary artery; acrodermatitis chronica atrophicans; acute cerebellar ataxia; adenocarcino...
ADR activation, depression, repetition [in bone remodeling]; adrenodoxin reductase; Adriamycin; adverse ...
AEM Academic Emergency Medicine [journal]; analytical electron microscopy; ambulatory electrocardiograph...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
AT Ataxia Telangiectasis
ATM Ataxia Telangiectasia Mutated
ADCA Autosomal Dominant Cerebellar Ataxia
FA Friedreich ataxia
FRDA Friedreich ataxia
Çѱ¹Ç¥ÁØÁúº´»çÀκзù ¾àÀÚ ¸ÂÃã °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
  • ÄÚµå
    ¿µ¹®
    ÇѱÛ
  • G11.9
    Hereditary ataxia, unspecified
    »ó¼¼ºÒ¸íÀÇ À¯Àü¼º ¿îµ¿½ÇÁ¶
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • unspecified
    ºñƯÀ̼º
    ´Ù¸¥ °ÍÇÏ°í¸¸ Ưº°È÷ °áÇÕÀ» ÇÑ´ÙµçÁö ¹ÝÀÀÇϴ ƯÀ̼ºÀÌ ¾ø´Â.
  • acute ataxia
    ±Þ¼º ¿îµ¿½ÇÁ¶
    ±ÙÀ° »óÈ£ÇùÁ¶°¡ °á¿©µÇ°Å³ª ±ÙÀ°±â´ÉÀÌ ºÒ±ÔÄ¢ÇÏ¿© ¿îµ¿±â´ÉÀÌ »ó½ÇµÇ´Â °Í.
  • dynamic ataxia
    ¿ªµ¿Àû ¿îµ¿ ½ÇÁ¶
  • Friedreich's ataxia
    Friedreich ¿îµ¿ ½ÇÁ¶Áõ
    ÀÓ»ó °æ°ú¿Í º´¸®ÇÐÀû ¼Ò°ßÀÌ ±Ô¸íµÇ¾î ÀÖÀ½¿¡µµ ºÒ±¸ÇÏ°í ¿À·§µ¿¾È ô¼ö-¼Ò³ú º¯¼ºÀ¸·Î¸¸ ÀÎ½ÄµÇ¾î ¿Ô´Ù. ÀÌ ÁúȯÀº »ó¿°»öü ¿­¼ºÀ¸·Î À¯ÀüµÇ¸ç ³²ÀÚ¿¡ ¸¹´Ù. ´ë°³ 11¼¼¿¡ ¹ßº´ÇÏ¸ç º¸Çà ½ÇÁ¶°¡ Ãʱâ Áõ»óÀÌ¸ç ¼Õ ¿òÁ÷ÀÓÀÌ ¼­Åø°í ±¸À½ Àå¾Ö°¡ µÚµû¸£°Ô µÈ´Ù. ½ÉºÎ °Ç ¹Ý»ç°¡ ¾ø¾îÁö³ª ½ÅÀü Á·Àú ¹Ý»ç´Â À¯ÁöµÈ´Ù. ´ëºÎºÐÀÇ È¯ÀÚ°¡ 20¿©³âÀÇ °æ°ú¸¦ °ÅÃÄ ¸¶ºñ »óÅ¿¡ À̸£°Ô µÈ´Ù. Å©¶óÅ© ÇÙ¿¡ ½Å°æ ¼¼Æ÷ ¼Ò½ÇÀÌ ÀÖ´Ù.
  • frontal ataxia
    ÀüµÎ¿±¼º ¿îµ¿½ÇÁ¶Áõ
  • frontal lobe ataxia
    ÀüµÎ¿± ½ÇÁ¶
  • juvenile ataxia
    ¿¬¼Ò¼º ¿îµ¿ ½ÇÁ¶, ¿¬¼Ò¼º ¿îµ¿ ½ÇÁ¶Áõ
  • labyrinthic ataxia
    ¹Ì·Î¼º ¿îµ¿ ½ÇÁ¶
  • ocular ataxia
    ¾È ÁøÅÁÁõ, ¾È±¸ ÁøÅÁÁõ
    µ¿ÀǾî=nystagmus.
  • hereditary
    À¯Àü¼º
    ºÎ¸ð·ÎºÎÅÍ ´ÙÀ½ ¼¼´ë·Î À¯ÀüÀÚ¿¡ ÀÇÇØ Àü´ÞµÇ´Â.
  • hereditary amyloidosis
    À¯Àü¼º À¯ÀüºÐÁõ
    1. À¯Àü¿¡ ÀÇÇØ ¿ø¼¶À¯¼º ´ç ´Ü¹éÀÌ ÇǺÎ, Á¡¸·, ³»ºÎ Àå±â¿¡ ħÀüµÇ´Â º´. 2. À¯ÀüÀûÀ¸·Î ½ÅüÀÇ °¢Á¾ ºÎÀ§¿¡ ¾Æ¹Ð·ÎÀ̵å
  • hereditary angioedema
    À¯Àü¼º ¸Æ°ü ºÎÁ¾, À¯Àü¼º Ç÷°ü ºÎÁ¾
    ½ÉºÎÀÇ ÁøÇÇ, ÇÇÇÏ Á¶Á÷, Á¡¸·ÇÏÁ¶Á÷À» ħ½ÀÇÏ´Â Ç÷°ü ¹ÝÀÀÀ¸·Î¼­, ¸ð¼¼Ç÷°üÀÇ È®Àå°ú Åõ°ú¼º Ç×Áø¿¡ ÀÇÇØ ÀϾ´Â ±¹ÇѼº ºÎÁ¾À» ³ªÅ¸³»¸ç °Å´ëÇÑ ÆØÁøÀÇ ¹ß»ýÀ» Ư¡À¸·Î ÇÑ´Ù. »ó¿°»öü¼º ¿ì¼º ÇüÁú·Î À¯ÀüÇÑ´Ù. »ê¹ß¼ºº¸´Ù ³»Àå º´º¯À» ´õ Àß ÀÏÀ¸Å°´Â °æÇâÀÌ ÀÖ´Ù.
  • hereditary aphasia
    À¯Àü ½Ç¾î, À¯Àü¼º ½Ç¾î, À¯Àü ½Ç¾îÁõ, À¯Àü¼º ½Ç¾îÁõ
  • hereditary brown tooth
    À¯Àü¼º °¥»ö Ä¡¾Æ
  • hereditary cerebrospinal paralysis
    ¿ìÀü¼º ³úô¼ö ¸¶ºñ
    º¸Åë Áß³â Ãʱ⿡ ÁøÇàÇÏ´Â À¯Àü¼º ÁúȯÀ¸·Î »óÁö ¶Ç´Â ÇÏÁöÀÇ ¾çÁö ¶Ç´Â ÀÏÃøÀ̳ª »çÁö¿¡ ³ªÅ¸³ª¸ç, ¼­¼­È÷ ÁøÇàµÇ´Â ¸¶ºñ°¡ Ư¡ÀÌ´Ù.
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
hereditary ataxia A simple autosomal recessive trait in fox terrier dogs that produces a progressive general ataxia.
(05 Mar 2000)
hereditary cerebellar ataxia A disease of later childhood and early adult life, marked by ataxic gait, hesitating and explosive speech, nystagmus, and sometimes optic neuritis. It probably comprises several distinct conditions with diverse patterns of inheritance.
Collective term for a number of hereditary disorders in which cerebellar signs are the most prominent finding.
(05 Mar 2000)
hereditary spinal ataxia Sclerosis of the posterior and lateral columns of the spinal cord, occurring in children and marked by ataxia in the lower extremities, extending to the upper, followed by paralysis and contractures; autosomal recessive inheritance.
See: spinocerebellar ataxia.
Synonym: Friedreich's ataxia, heredotaxia.
(05 Mar 2000)
acute ataxia Generalised ataxia of abrupt onset, most often caused by drug intoxications, poisonings, or vestibular neuronitis.
(05 Mar 2000)
ataxia <neurology> Failure of muscular coordination, irregularity of muscular action.
Origin: Gr. Taxis = order
(16 Dec 1997)
ataxia cordis <cardiology> A condition where there is disorganised electrical conduction in the atria, resulting in ineffective pumping of blood into the ventricle.
Acronym: AF
(02 Jan 1998)
ataxia of calves A specific cerebellar ataxia in the Jersey breed, probably a recessive genetic trait.
(05 Mar 2000)
ataxia of lambs Myelination failure seen in ewes on a copper-deficient diet.
(05 Mar 2000)
ataxia-telangiectasia <neurology, oncology> An intriguing autosomal recessive disorder in which a single defective gene produces myriad and protean effects, presents with cerebellar ataxia, telangiectasias in the eyes and skin, immune deficiency and autoimmune phenomena, propensity for lymphoid and other malignancies, excessive sensitivity to ionising radiation, increased serum alpha-fetoprotein concentrations and a tendency for chromosome breakage and translocation.
A syndrome characterised by choreoathetosis beginning in childhood, progressive cerebellar ataxia, telangiectasis of conjunctiva and skin, slowly progressive mental deterioration and increasing cerebellar degeneration.
There is evidence that heterozygotes show an increased susceptibility to malignancy as well, with breast cancer often cited. The gene was localised by linkage studies to chromosome 11q22-23, and recently cloned, revealing it to be homologous to the PI-3 kinase family so that prenatal diagnosis by RFLP analysis is possible.
Other related genes are suspected to exist. Diagnosis in affected patients is made on clinical grounds, by detection of high concentrations of alpha-fetoprotein, and by a specialised cell culture assay for radiosensitivity and atypical radioresistant DNA synthesis. These cell culture methods are also used for prenatal diagnosis.
A characteristic autopsy feature of ataxia-telangiectasia is the presence of empty basket cells in the cerebellum which results from degeneration of the previously contained Purkinje cells.
Inheritance: autosomal recessive.
(16 Dec 1998)
ataxia telangiectasia syndrome ataxia telangiectasia
bovine congenital ataxia An autosomal recessive ataxia seen in several European breeds of cattle.
(05 Mar 2000)
Briquet's ataxia Weakening of the muscle sense and increased sensibility of the skin, in hysteria.
Synonym: hysterical ataxia.
(05 Mar 2000)
Bruns ataxia Difficulty in initiation of movements of the feet when they are in contact with the ground; a condition related to a frontal lobe lesion.
(05 Mar 2000)
vasomotor ataxia A form of autonomic ataxia causing irregularity in the peripheral circulation, marked by alternations of pallor and suffusion, due to spasm of the smaller blood vessels.
(05 Mar 2000)
Marie's ataxia An obsolete term for a variety of non-Friedreich hereditary ataxias.
(05 Mar 2000)
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  • ¿µ¹®
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  • unspecified
    Ư±â
  • ataxia
    ¿îµ¿ ½ÇÁ¶(ƯÈ÷ ¼Õ¹ßÀÇ)
  • locomotor ataxia
    ¿îµ¿Àå¾Ö
  • hereditary
    À¯Àü¼ºÀÇ; ¼¼½ÀÀÇ
  • hereditary
    À¯ÀüÀÇ;¼¼½ÀÀÇ;´ë´ëÀÇ
  • hereditary peer
    ¼¼½À ±ÍÁ·
ÀÌ ¾Æ·¡ ºÎÅÍ´Â °á°ú°¡ ¾ø½À´Ï´Ù.
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    ±¸ºÐ/º¸Çè±Þ¿©
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