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Familiar ataxia
Friedreich's spinal ataxia
Hereditary spinal ataxia 2.Friedreich's disease
Marie ataxia
Marie's ataxia
Marie's cerebellar ataxia
SCA1
SCA2
SCA7
SCAR2
Spinocerebellar ataxia
Spinocerebellar ataxia 1
Spinocerebellar ataxia 2
Spinocerebellar ataxia 7
Spinocerebellar ataxia II
Spinocerebellar ataxia type 1
Spinocerebellar ataxia type 2
Type 1 spinocerebellar ataxia

Traduction de «Spinocerebellar ataxia II » (Anglais → Français) :

spinocerebellar ataxia 2 | SCA2 | spinocerebellar ataxia type 2 | spinocerebellar ataxia II

ataxie spinocérébelleuse 2 | SCA2


spinocerebellar ataxia 1 | SCA1 | type 1 spinocerebellar ataxia | spinocerebellar ataxia type 1

ataxie spinocérébelleuse 1 | ataxie spinocérébellaire 1 | ataxie spino-cérébelleuse de type I | ataxie spinocérébelleuse de type 1 | SCA 1




SCAR2 (spinocerebellar ataxia autosomal recessive 2)

ataxie cérébelleuse autosomique récessive type 3




spinocerebellar ataxia 7 | SCA7

ataxie spinocérébelleuse 7 | SCA 7


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


Spinocerebellar ataxia type 31 (SCA31) is a very rare disease with manifestation of late-onset of cerebral ataxia, dysarthria, and horizontal gaze nystagmus, and that is occasionally accompanied by pyramidal signs, tremor, decreased vibration sense,

ataxie spinocérébelleuse type 31


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

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


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

hérédo-ataxie cérébelleuse de Pierre Marie




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Date index: 2021-08-31
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