Traduction de «congenitale niet-progressieve spinocerebellaire ataxie » (Néerlandais → Anglais) :

congenitale niet-progressieve spinocerebellaire ataxie
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

autosomaal recessieve traag progressieve spinocerebellaire ataxie beginnend op kinderleeftijd
Autosomal recessive spinocerebellar ataxia type 7

X-gebonden niet-progressieve cerebellaire ataxie
A rare hereditary ataxia with characteristics of delayed early motor development, severe neonatal hypotonia, non-progressive ataxia and slow eye movements, presenting normal cognitive abilities and absence of pyramidal signs. Frequently patients also

congenitale ataxie, niet progressief
Congenital nonprogressive ataxia