Review Note
Last Update: 12/09/2024 11:18 AM
Current Deck: BUMed Mother Deck::YL2.S1-PATHOLOGY::PTH.S1.L14.Diseases of Infancy and Childhood::IV. Hydrops to PKU
PublishedCurrently Published Content
Front
Autosomal recessive disorder caused by severe deficiency of the
enzyme phenylalanine hydroxylase (PAH) leading to
hyperphenylalaninemia
enzyme phenylalanine hydroxylase (PAH) leading to
hyperphenylalaninemia
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PHENYLKETONURIA
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