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Translation of "Early-onset cerebellar ataxia with essential tremor " (English → French) :
TERMINOLOGY
see also In-Context Translations below 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
EOCA - Early onset cerebellar ataxia with retained tendon reflexes
ataxie de Harding
SNOMEDCT-BE (disorder) / 230228004
SNOMEDCT-BE (disorder) / 230228004
Early onset cerebellar ataxia with retained tendon reflexes
ataxie cérébelleuse précoce avec conservation des réflexes tendineux
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
A rare subtype of type 1 autosomal dominant cerebellar ataxia with characteristics of cerebellar ataxia, tremor and cognitive impairment. Prevalence is unknown. Fewer than 80 patients affected by the disease have been identified to date. Age of onset
ataxie spinocérébelleuse type 15/16
SNOMEDCT-BE (disorder) / 716724006
SNOMEDCT-BE (disorder) / 716724006
Disease with characteristics of early-onset of cerebellar signs with eye movement abnormalities and a very slow disease progression.Three families have been reported to date. Clinical manifestations include cerebellar signs (ataxia, dysarthria, and i
ataxie spinocérébelleuse type 5
SNOMEDCT-BE (ataxia, dysarthria, and i / 719302009
SNOMEDCT-BE (disorder) / 719302009
A genetic neurodegenerative disease with normal early development followed by childhood onset optic atrophy with progressive vision loss and eventually blindness, followed by progressive neurological decline that typically includes cerebellar ataxia,
syndrome de neurodégénérescence progressive de l'enfant-cécité-ataxie-spasticité
SNOMEDCT-BE (disorder) / 771514002
SNOMEDCT-BE (disorder) / 771514002
An inherited epileptic syndrome characterized by cortical hand tremors, myoclonic jerks and occasional generalized or focal seizures with a non-progressive or very slowly progressive disease course, and no signs of early dementia or cerebellar ataxia
ADCME - autosomal dominant cortical myoclonus and epilepsy
SNOMEDCT-BE (disorder) / 717225001
SNOMEDCT-BE (disorder) / 717225001
This disease has characteristics of progressive cerebellar ataxia with pyramidal and spinal cord dysfunction, associated with distinctive MRI anomalies and increased lactate in the abnormal white matter. Onset occurs in early childhood. Epilepsy and
syndrome de leucoencéphalopathie avec atteinte du tronc cérébral et de la moelle épinière-élévation des lactates
SNOMEDCT-BE (disorder) / 735421004
SNOMEDCT-BE (disorder) / 735421004
www.wordscope.com (v4.0.br.77)
'Early-onset cerebellar ataxia with essential tremor'
Date index:2023-08-20 -
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