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Familiar ataxia
Friedreich ataxia
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
Friedreich's spinal ataxia
Hereditary ataxia
Hereditary spinal ataxia 2.Friedreich's disease
Other hereditary ataxias

Translation of "Friedreich's hereditary ataxia " (English → French) :

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


familiar ataxia | Friedreich's spinal ataxia | hereditary spinal ataxia 2.Friedreich's disease

ataxie de Friedreich | ataxie héréditaire | maladie de Friedreich | tabes héréditaire
IATE - Health
IATE - Health


Friedreich's ataxia

maladie de Friedreich
médecine
médecine


A rare hereditary ataxia with characteristics of progressive cerebellar ataxia associated with disruption of visual fixation by saccadic intrusions. It presents with progressive gait, trunk and limb ataxia with pyramidal tract signs (increased tendon

syndrome d'ataxie cérébelleuse autosomique récessive-saccade oculaire
SNOMEDCT-BE (increased tendon / 766814006
SNOMEDCT-BE (disorder) / 766814006


A rare hereditary ataxia characterized by recurrent episodes of ataxia with variable frequency and duration, associated with slurred speech, generalized muscle weakness and balance disturbance. Other symptoms may occur between episodes, including int

ataxie épisodique avec troubles de l'élocution
SNOMEDCT-BE (disorder) / 773495009
SNOMEDCT-BE (disorder) / 773495009


A rare hereditary ataxia with characteristics of delayed early motor development, severe neonatal hypotonia, non-progressive ataxia and slow eye movements, presenting normal cognitive abilities and absence of pyramidal signs. Frequently patients also

ataxie cérébelleuse liée à l'X non progressive
SNOMEDCT-BE (disorder) / 766818009
SNOMEDCT-BE (disorder) / 766818009


Hereditary ataxia

Ataxie héréditaire
WORLD HEALTH ORGANIZATION ICD-10: G11
WORLD HEALTH ORGANIZATION ICD-10: G11


Other hereditary ataxias

Autres ataxies héréditaires
WORLD HEALTH ORGANIZATION ICD-10: G11.8
WORLD HEALTH ORGANIZATION ICD-10: G11.8


Friedreich's ataxia

ataxie de Friedreich
IATE - Health
IATE - Health


Friedreich ataxia

maladie de Friedreich
IATE - Health
IATE - Health




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Friedreich's hereditary ataxia

Date index:2024-04-06 -

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