181: A patient with pyruvate carboxylase deficiency

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Pyruvate carboxylase deficiency: mechanisms, mimics and anaplerosis.

Pyruvate carboxylase (PC) is a regulated mitochondrial enzyme that catalyzes the conversion of pyruvate to oxaloacetate, a critical transition that replenishes citric acid cycle intermediates and facilitates other biosynthetic reactions that drive anabolism. Its deficiency causes multiorgan metabolic imbalance that predominantly manifests with lactic acidemia and neurological dysfunction at an ...

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Pyruvate carboxylase deficiency: An underestimated cause of lactic acidosis

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ژورنال

عنوان ژورنال: Pediatric Research

سال: 1976

ISSN: 0031-3998,1530-0447

DOI: 10.1203/00006450-197610000-00172