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Early-onset cerebellar ataxia
Early-onset cerebellar ataxia with essential tremor
Hunt's ataxia
Late-onset cerebellar ataxia
Myoclonus
Retained tendon reflexes

Translation of "late-onset cerebellar ataxia " (English → French) :

Late-onset cerebellar ataxia

Ataxie cérébelleuse tardive
WORLD HEALTH ORGANIZATION ICD-10: G11.2
WORLD HEALTH ORGANIZATION ICD-10: G11.2


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
WORLD HEALTH ORGANIZATION ICD-10: G11.1
WORLD HEALTH ORGANIZATION ICD-10: G11.1


Early-onset cerebellar ataxia

Ataxie cérébelleuse à début précoce
WORLD HEALTH ORGANIZATION ICD-10: G11.1
WORLD HEALTH ORGANIZATION ICD-10: G11.1


Early onset cerebellar ataxia with retained tendon reflexes

ataxie cérébelleuse précoce avec conservation des réflexes tendineux
SNOMEDCT-BE (disorder) / 230228004
SNOMEDCT-BE (disorder) / 230228004


EOCA - Early onset cerebellar ataxia with retained tendon reflexes

ataxie de Harding
SNOMEDCT-BE (disorder) / 230228004
SNOMEDCT-BE (disorder) / 230228004


A very rare subtype of autosomal dominant cerebellar ataxia type 3 with characteristics of late-onset and slowly progressive cerebellar signs (gait ataxia) and eye movement abnormalities. To date, only 23 affected patients have been described from on

ataxie spinocérébelleuse type 26
SNOMEDCT-BE (gait ataxia) and eye movement abnormalities. To date, only 23 affected patients have been described from on / 718769009
SNOMEDCT-BE (disorder) / 718769009




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'late-onset cerebellar ataxia'

Date index:2023-12-19 -

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