Traduction de «acute cerebellar ataxia » (Anglais → Néerlandais) :

acute cerebellar ataxia
ataxia cerebellaris

congenital cerebellar ataxia | Marie disease | Marie's cerebellar ataxia | Marie's disease | Nonne-Marie sydrome
erfelijke cerebellaire ataxie

Marie ataxia | Marie's ataxia | Marie's cerebellar ataxia
cerebellaire heredo-ataxie

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
spinocerebellaire ataxie type 26

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
spinocerebellaire ataxie type 28

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
cerebellaire ataxie, Cayman-type

Early-onset cerebellar ataxia with:essential tremor | myoclonus [Hunt's ataxia] | retained tendon reflexes | Friedreich's ataxia (autosomal recessive) X-linked recessive spinocerebellar ataxia
Friedreich-ataxie (autosomaal recessief) | vroeg optredende cerebellaire ataxie met | behouden peesreflexen | vroeg optredende cerebellaire ataxie met | essentiële tremor | vroeg optredende cerebellaire ataxie met | myoclonus [Hunts ataxie] | recessieve spinocerebellaire ataxie, X-gebonden

Late-onset cerebellar ataxia
laat-optredende cerebellaire ataxie

Early-onset cerebellar ataxia
vroeg optredende cerebellaire ataxie