Vertaling van "Alcoholic cerebellar ataxia " (Engels → Frans) :

Alcoholic:cerebellar:ataxia | degeneration | cerebral degeneration | encephalopathy | Dysfunction of autonomic nervous system due to alcohol
Ataxie cérébelleuse | Dégénérescence cérébelleuse | Dégénérescence cérébrale | Dysautonomie | Encéphalopathie | alcoolique

congenital cerebellar ataxia | Marie disease | Marie's cerebellar ataxia | Marie's disease | Nonne-Marie sydrome
hérédo-ataxie cérébelleuse

Marie ataxia | Marie's ataxia | Marie's cerebellar ataxia
hérédo-ataxie cérébelleuse de Pierre Marie

Cerebellar ataxia Cayman type has characteristics of psychomotor retardation, hypotonia and cerebellar dysfunction (nystagmus, ataxic gait, truncal ataxia, dysarthric speech and intention tremor), associated with cerebellar hypoplasia. The prevalence
ataxie type Caïman

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

A very rare subtype of autosomal dominant cerebellar ataxia type 3 with characteristics of late-onset and slowly progressive cerebellar signs (gait ataxia) and eye movement abnormalities. To date, only 23 affected patients have been described from on
ataxie spinocérébelleuse type 26

cerebellar ataxia
ataxie cérébelleuse

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

acute cerebellar ataxia
ataxie cérébelleuse aiguë

Early-onset cerebellar ataxia
Ataxie cérébelleuse à début précoce