#pyruvate_dehydrogenase_deficiency
Pyruvate dehydrogenase deficiency
Medical condition
Pyruvate dehydrogenase deficiency is a rare neurodegenerative disorder associated with abnormal mitochondrial metabolism. PDCD is a genetic disease resulting from mutations in one of the components of the pyruvate dehydrogenase complex (PDC). The PDC is a multi-enzyme complex that plays a vital role as a key regulatory step in the central pathways of energy metabolism in the mitochondria. The disorder shows heterogeneous characteristics in both clinical presentation and biochemical abnormality.
Wed 11th
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Pyruvate dehydrogenase deficiency Pyruvate dehydrogenase complex Pyruvate dehydrogenase Dihydrolipoyl transacetylase Pyruvate dehydrogenase (lipoamide) alpha 1 Pyruvate dehydrogenase (lipoamide) beta Pyruvate dehydrogenase phosphatase Pyruvate dehydrogenase kinase Lactate dehydrogenase Glucose-6-phosphate dehydrogenase deficiency
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