Vertaling van "friedreich familial ataxia " (Engels → Frans) :

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 ]

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

Friedreich's ataxia
maladie de Friedreich

Canadian Association of Familial Ataxias [ Canadian Association of Friedrich's Ataxia ]
Association Canadienne des Ataxies Familiales [ ACAF | Association canadienne de l'Ataxie de Friedreich ]

Friedreich's ataxia
ataxie de Friedreich

Friedreich-like ataxia
ataxie par déficit en vitamine E

familiar ataxia | Friedreich's spinal ataxia | hereditary spinal ataxia 2.Friedreich's disease
ataxie de Friedreich | ataxie héréditaire | maladie de Friedreich | tabes héréditaire

Friedreich ataxia
maladie de Friedreich

A rare disease with characteristics of slowly progressive and relatively pure ataxia described in 6 patients from one Australian family to date. The disease presents with oculomotor dysfunction, moderate dysarthria, and ataxia that progresses slowly
ataxie spinocérébelleuse type 30

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