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PedAM

Pediatric Disease Annotations & Medicines




Disease myopathy
Phenotype C0020598|hypoglycemia
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PubMedID- 20301700 The three recognized phenotypes are hepatic encephalopathy, in which individuals (typically children) present with hypoketotic hypoglycemia and sudden onset of liver failure; adult-onset myopathy, seen in one individual of inuit origin; and acute fatty liver of pregnancy, in which the fetus is homozygous for a pathogenic variant in cpt1a that causes cpt1a deficiency.

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