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

Translation of "Early-onset cerebellar ataxia with essential tremor " (English → French) :

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 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


Disease with characteristics of early-onset tremor, dyskinesia and slowly progressive cerebellar ataxia. Fewer than 30 cases have been reported to date. This disease is caused by a mutation in the fibroblast growth factor 14 FGF14 gene (13q34). Progn

ataxie spinocérébelleuse type 27
SNOMEDCT-BE (13q34). Progn / 719252002
SNOMEDCT-BE (disorder) / 719252002




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'Early-onset cerebellar ataxia with essential tremor'

Date index:2023-11-22 -

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