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xanthurenic aciduria - translation to arabic
PYRIMIDINE METABOLIC DISORDER THAT IS CHARACTERIZED BY AN EXCESSIVE SECRETION OF OROTIC ACID IN URINE
Orotic aciduria hereditary; Orotic aciduria purines-pyrimidines; Hereditary orotic aciduria
xanthurenic aciduria
بِيلَةُ حَمْضِ الزنتورينيك
orotic aciduria
بِيلَةُ حَمْضِ الأوروتيك
glutaric aciduria
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
Glutaryl-CoA dehydrogenase deficiency; Glutaric acidemia I; Glutaric aciduria I; Glutaric acidemia type I; Glutaric aciduria; Glutaric acidemia type 1; Glutari aciduria; Glutaric acidemia
بِيلَةُ حَمْضِ الغلُوتاريك
Wikipedia
Orotic aciduria
Orotic aciduria (AKA hereditary orotic aciduria) is a disease caused by an enzyme deficiency, resulting in a decreased ability to synthesize pyrimidines. It was the first described enzyme deficiency of the de novo pyrimidine synthesis pathway.
Orotic aciduria is characterized by excessive excretion of orotic acid in urine because of the inability to convert orotic acid to UMP. It causes megaloblastic anemia and may be associated with mental and physical developmental delays.
