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    ÇѱÛ
  • hereditary cerebellar ataxia
    À¯Àü¼Ò³ú½ÇÁ¶
  • locomotor ataxia
    À̵¿½ÇÁ¶
  • sensory ataxia
    °¨°¢¼º½ÇÁ¶
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 1 ÆäÀÌÁö: 2
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    ÇѱÛ
  • sensory ataxia
    °¨°¢¼ºÁ¶È­¿îµ¿ºÒ´É
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  • ¿µ¹®
    ÇѱÛ
  • 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).
  • 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)
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VMR vasomotor rhinitis
VMT vasomotor tonus; ventilatory muscle training; ventromedial tegmentum
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...
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FRDA Friedreich ataxia
SCA1 Spinocerebellar Ataxia 1
SCA2 Spinocerebellar Ataxia Type 2
SCA Spinocerebellar ataxia
SCA-2 Spinocerebellar ataxia 2
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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)
Marie's ataxia An obsolete term for a variety of non-Friedreich hereditary ataxias.
(05 Mar 2000)
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)
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