Cerebellar ataxia Cayman type has characteristics of psychomotor retardation, hypotonia and cerebellar dysfunction (nystagmus, ataxic gait, truncal ataxia, dysarthric speech and intention tremor), associated with cerebellar hypoplasia. The prevalence

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ataxie type Caïman

SNOMEDCT-BE (disorder) / 717332007

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ataxie de Friedreich [ maladie de Friedreich | ataxie héréditaire ]

Nervous System

Système nerveux

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vestibular ataxia [ labyrinthic ataxia | labyrinthine ataxia ]

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ataxie labyrinthique [ ataxie vestibulaire ]

Nervous System

Système nerveux

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spinocerebellar ataxia 1 | SCA1 | type 1 spinocerebellar ataxia | spinocerebellar ataxia type 1

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ataxie spinocérébelleuse 1 | ataxie spinocérébellaire 1 | ataxie spino-cérébelleuse de type I | ataxie spinocérébelleuse de type 1 | SCA 1

médecine > sémiologie et pathologie | médecine > neurologie | biologie > génétique

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spinocerebellar ataxia 2 | SCA2 | spinocerebellar ataxia type 2 | spinocerebellar ataxia II

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ataxie spinocérébelleuse 2 | SCA2

médecine > sémiologie et pathologie | médecine > neurologie | biologie > génétique

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familiar ataxia | Friedreich's spinal ataxia | hereditary spinal ataxia 2.Friedreich's disease

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ataxie de Friedreich | ataxie héréditaire | maladie de Friedreich | tabes héréditaire

IATE - Health

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Louis-Bar syndrome | Boder-Sedgwick syndrome | ataxia-telangiectasia | ataxia teleangiectasica | cephalo-oculocutaneous telangiectasis

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syndrome de Louis-Bar | ataxie | télangiectasie | syndrome de Mme Louis-Bar

biologie > génétique | médecine > neurologie

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Canadian Association of Familial Ataxias [ Canadian Association of Friedrich's Ataxia ]

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Association Canadienne des Ataxies Familiales [ ACAF | Association canadienne de l'Ataxie de Friedreich ]

Private-Sector Bodies and Committees | Nervous System

Organismes et comités du secteur privé | Système nerveux

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Disease with characteristics of the adult-onset (average age 40 years) of truncal ataxia, gait disturbance and gaze-evoked nystagmus. The disease is slowly progressive with dysarthria and limb ataxia following. Additional manifestations include diplo

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ataxie spinocérébelleuse type 38

SNOMEDCT-BE (average age 40 years) of truncal ataxia, gait disturbance and gaze-evoked nystagmus. The disease is slowly progressive with dysarthria and limb ataxia following. Additional manifestations include diplo / 734021001

SNOMEDCT-BE (disorder) / 734021001

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Others have searched : boder-sedgwick syndrome canadian association of familial ataxias canadian association of friedrich's ataxia cayman ataxia friedreich disease friedreich familial ataxia friedreich hereditary ataxia friedreich hereditary spinal ataxia friedreich spinocerebella friedreich's ataxia friedreich's disease friedreich's familial ataxia friedreich's hereditary ataxia friedreich's hereditary spinal ataxia friedreich's spinal ataxia louis-bar syndrome ataxia teleangiectasica familiar ataxia labyrinthic ataxia labyrinthine ataxia spinocerebellar ataxia spinocerebellar ataxia ii spinocerebellar ataxia type type 1 spinocerebellar ataxia vestibular ataxia

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'cayman ataxia'

Date index:2021-12-03 -

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Translation of "cayman ataxia " (English → French) :

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