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Ataxia teleangiectasica
Ataxia-telangiectasia
Boder-Sedgwick syndrome
Canadian Association of Familial Ataxias
Canadian Association of Friedrich's Ataxia
Cayman ataxia
Cephalo-oculocutaneous telangiectasis
Familiar 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
Hereditary spinal ataxia 2.Friedreich's disease
Labyrinthic ataxia
Labyrinthine ataxia
Louis-Bar syndrome
SCA1
SCA2
Spinocerebellar ataxia 1
Spinocerebellar ataxia 2
Spinocerebellar ataxia II
Spinocerebellar ataxia type 1
Spinocerebellar ataxia type 2
Type 1 spinocerebellar ataxia
Vestibular ataxia

Traduction de «cayman ataxia » (Anglais → Français) :



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

ataxie type Caïman


Friedreich's ataxia [ Friedreich's disease | Friedreich disease | Friedreich's hereditary spinal ataxia | Friedreich hereditary spinal ataxia | Friedreich familial ataxia | Friedreich's familial ataxia | Friedreich hereditary ataxia | Friedreich's hereditary ataxia | Friedreich spinocerebella ]

ataxie de Friedreich [ maladie de Friedreich | ataxie héréditaire ]


vestibular ataxia [ labyrinthic ataxia | labyrinthine ataxia ]

ataxie labyrinthique [ ataxie vestibulaire ]


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

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


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

ataxie spinocérébelleuse 2 | SCA2


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

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


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

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


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

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


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

ataxie spinocérébelleuse type 38


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