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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

Traduction de «friedreich's hereditary ataxia » (Anglais → Français) :

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 ]


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

ataxie de Friedreich | ataxie héréditaire | maladie de Friedreich | tabes héréditaire




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


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


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












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Date index: 2023-04-13
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