Fig. 2From: Severe clinical manifestation of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency associated with two novel mutations: a case reportChromatogram of urine organic acids from our patient. Urine was sampled during an acute episode of metabolic disturbance involving acidosis. The results indicate significant elevation of 3-hydroxybutyric acid, glutaric acid, adipic acid glycerol; as well as moderate elevation of dicarboxylic acids, 3-hydroxydicarboxylic acids, 4-hydroxyphenyllactate acidsBack to article page