Vertaling van "spinocerebellar ataxia type " (Engels → Frans) :

Spinocerebellar ataxia type 29 (SCA29) is a rare disease with main features of very slowly progressive or non-progressive ataxia, dysarthria, oculomotor abnormalities and intellectual disability. SCA29 presents at birth, or shortly, after with manife
ataxie spinocérébelleuse type 29

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

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

spinocerebellar ataxia 2 | SCA2 | spinocerebellar ataxia type 2 | spinocerebellar ataxia II
ataxie spinocérébelleuse 2 | SCA2

spinocerebellar ataxia
ataxie spinocérébelleuse

spinocerebellar ataxia 7 | SCA7
ataxie spinocérébelleuse 7 | SCA 7

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