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Acute cerebellar ataxia
Cerebellar ataxia
Congenital cerebellar ataxia
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
Marie ataxia
Marie disease
Marie's ataxia
Marie's cerebellar ataxia
Marie's disease
Myoclonus
Nonne-Marie sydrome
Retained tendon reflexes
Vestibular ataxia

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

TERMINOLOGY
see also In-Context Translations below
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
SNOMEDCT-BE (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 / 715824008
SNOMEDCT-BE (disorder) / 715824008


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
SNOMEDCT-BE (disorder) / 717332007
SNOMEDCT-BE (disorder) / 717332007


cerebellar ataxia

ataxie cérébelleuse
Nervous System
Système nerveux


acute cerebellar ataxia

ataxie cérébelleuse aiguë
IATE - Health
IATE - Health


congenital cerebellar ataxia | Marie disease | Marie's cerebellar ataxia | Marie's disease | Nonne-Marie sydrome

rédo-ataxie cérébelleuse
IATE - Health
IATE - Health


Marie ataxia | Marie's ataxia | Marie's cerebellar ataxia

hérédo-ataxie cérébelleuse de Pierre Marie
IATE - Health
IATE - Health


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


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


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 ]
Nervous System
Système nerveux


vestibular ataxia [ labyrinthic ataxia | labyrinthine ataxia ]

ataxie labyrinthique [ ataxie vestibulaire ]
Nervous System
Système nerveux
IN-CONTEXT TRANSLATIONS
Moreover, these bananas are produced in Ecuador by 10-year-old children who are paid USD 2 a day, who inhale pesticides, who have asthma, who have problems with their balance and who suffer from cerebellar ataxia.

Par ailleurs, ces bananes sont produites en Équateur par des enfants de dix ans qui sont payés 2 dollars par journée, qui inhalent des pesticides, qui ont de l’asthme, qui ont des troubles de l’équilibre, qui souffrent d’ataxie cérébelleuse.




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'cerebellar ataxia'

Date index:2024-01-11 -

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