Vertaling van "dentate cerebellar ataxia " (Engels → Nederlands) :

Dentate cerebellar ataxia
dyssynergia cerebellaris myoclonica

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

dentate cerebellar nucleus | dentate nucleus | rhomboid body
corpus dentatum | corpus dentatum cerebelli | corpus rhomboidale | nucleus cerebelli | nucleus dentatus

dentate cerebellar nucleus | dentate nucleus
corpus dentatum | corpus dentatum cerebelli | corpus rhomboidale | nucleus cerebelli | nucleus dentatus

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

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

Early-onset cerebellar ataxia
vroeg optredende cerebellaire ataxie

Late-onset cerebellar ataxia
laat-optredende cerebellaire ataxie