Open main menu
glutaric aciduria type 1 
Glutaryl-CoA dehydrogenase (GCDH) deficiency (GDD) is an autosomal recessive neurometabolic disorder clinically characterized by encephalopathic crises resulting in striatal injury and a severe dystonic dyskinetic movement disorder
Glutaric acid.png
Upload media
Wikipedia-logo-v2.svg  Wikipedia
Instance of disease
Subclass of cerebral organic aciduria,
neurometabolic disease
Authority control
Blue pencil.svg
Aciduria glutárica tipo I (es); グルタル酸尿症1型 (ja); acidurie glutarique type 1 (fr); Glutarsyreuri typ 1 (sv); Acyduria glutarowa typu I (pl); Glutaaracidurie type 1 (nl); Glutarazidurie Typ 1 (de); glutaric aciduria type 1 (en); گلوتاریک اسیدوری نوع یک (fa); Γλουταρική οξυουρία τύπου 1 (el) Glutaryl-CoA dehydrogenase (GCDH) deficiency (GDD) is an autosomal recessive neurometabolic disorder clinically characterized by encephalopathic crises resulting in striatal injury and a severe dystonic dyskinetic movement disorder (en) Aciduria glutarica tipo I (es); Glutaryl-CoA-Dehydrogenase-Defizienz (de); Déficit en glutaryl-CoA déshydrogénase (fr); glutaryl-CoA dehydrogenase deficiency, GA1, glutaric acidemia type 1, GCDHD, GLUTARIC ACIDEMIA I, Glutaryl-coenzyme A dehydrogenase deficiency, Glutaric Aciduria 1, Ga 1, Glutaric Aciduria, Type 1, Glutaric aciduria type 1 (en)

Media in category "Glutaric aciduria type 1"

The following 2 files are in this category, out of 2 total.