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Early-onset cerebellar ataxia with essential tremor
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
Hunt's ataxia
Labyrinthic ataxia
Labyrinthine ataxia
Myoclonus
Retained tendon reflexes
SCA1
SCA2
SCA7
SCAR2
Spinocerebellar ataxia
Spinocerebellar ataxia 1
Spinocerebellar ataxia 2
Spinocerebellar ataxia 7
Spinocerebellar ataxia II
Spinocerebellar ataxia type 1
Spinocerebellar ataxia type 2
Type 1 spinocerebellar ataxia
Vestibular ataxia

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

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

ataxie spinocérébelleuse 2 | SCA2


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


SCAR2 (spinocerebellar ataxia autosomal recessive 2)

ataxie cérébelleuse autosomique récessive type 3


spinocerebellar ataxia 7 | SCA7

ataxie spinocérébelleuse 7 | SCA 7




Spinocerebellar ataxia type 28 (SCA28) is very rare with main features of juvenile onset and slowly progressive cerebellar ataxia due to Purkinje cell degeneration. The mean age of symptom onset was 19.5 years in the original kindred. Some patients s

ataxie spinocérébelleuse type 28


Spinocerebellar ataxia type 31 (SCA31) is a very rare disease with manifestation of late-onset of cerebral ataxia, dysarthria, and horizontal gaze nystagmus, and that is occasionally accompanied by pyramidal signs, tremor, decreased vibration sense,

ataxie spinocérébelleuse type 31


Early-onset cerebellar ataxia with:essential tremor | myoclonus [Hunt's ataxia] | retained tendon reflexes | Friedreich's ataxia (autosomal recessive) X-linked recessive spinocerebellar ataxia

Ataxie (de):cérébelleuse précoce avec:myoclonies [Ramsay-Hunt] | persistance des réflexes tendineux | tremblement essentiel | Friedreich (autosomique récessive) | spino-cérébelleuse récessive liée au chromosome X


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 ]


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