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"Marie ataxia"¿¡ ´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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  • 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¶.
  • 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).
  • hysterical ataxia
    È÷½ºÅ׸®¼º ¿îµ¿½ÇÁ¶
  • hysterical ataxia
    È÷½ºÅ׸®¼º ¿îµ¿½ÇÁ¶.
  • juvenile ataxia
    ¿¬¼Ò¼º ¿îµ¿½ÇÁ¶(Áõ).
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 2
MS Maffuci syndrome; maladjustment score; mandibular series; Marfan syndrome; Marie-Strumpell [syndrome...
SM Master of Science; sadomasochism; self-monitoring; silicon microphysiometer; simple mastectomy; skim...
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: 2
CMT1A Charcot-Marie-Tooth Type 1A
CMT-X Charcot-Marie-Tooth disease
AT Ataxia Telangiectasis
ATM Ataxia Telangiectasia Mutated
ADCA Autosomal Dominant Cerebellar Ataxia
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
Poiseuille, Jean Leonard Marie <person> French physiologist and physicist, 1797-1869.
See: poise, Poiseuille's viscosity coefficient, Poiseuille's law, Poiseuille's space.
(05 Mar 2000)
Strumpell-Marie disease <rheumatology> A polyarthritis involving the spine, which is characterised by progressive, painful stiffening of the joints and ligaments. It almost exclusively affects young men.
Interestingly the disease seems to be associated with HLA B27, those with this histocompatability antigen are 300 times more likely to get the disease, 90% of sufferers have HLA B27
(18 Nov 1997)
Joubert, Marie <person> 20th century Canadian neurologist.
See: Joubert's syndrome.
(05 Mar 2000)
Foix-Cavany-Marie syndrome <syndrome> Constellation of facio-pharyngo-glosso-masticatory diplegia with automatic voluntary dissociation without associated dementia or forced laughing or crying usually caused by bilateral large artery infarcts of the opercular cortex.
(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)
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