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Early-onset cerebellar ataxia with essential tremor
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
Friedreich-like ataxia
Hereditary spinal ataxia 2.Friedreich's disease
Hunt's ataxia
Myoclonus
Retained tendon reflexes
Spinal ataxia

Translation of "Friedreich's spinal 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




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 ataxia

maladie de Friedreich
IATE - Health
IATE - Health


Friedreich-like ataxia

ataxie par déficit en vitamine E
SNOMEDCT-BE (disorder) / 702442008
SNOMEDCT-BE (disorder) / 702442008


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




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Friedreich's spinal ataxia

Date index:2022-05-22 -

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