Tetrahydrobiopterin-responsive hyperphenylalaninemia/phenylketonuria

MONDO:0017389

Tetrahydrobiopterin-responsive hyperphenylalaninemia/ phenylketonuria (BH4-responsive hyperphenylalaninemia/ phenylketonuria) is a form of phenylketonuria (PKU), an inborn error of amino acid metabolism, characterized by mild to moderate symptoms of PKU including impaired cognitive function, seizures, and behavioral and developmental disorders, and a marked reduction and normalization of elevated phenylalanine concentrations after oral loading with tetrahydrobiopterin (BH4; sapropterin dihydrochloride), an essential cofactor of phenylalanine hydroxylase.

Also known as: BH4-responsive HPA/PKU, BH4-responsive hyperphenylalaninemia/phenylketonuria, tetrahydrobiopterin-responsive HPA/PKU

24 clinical trials for this condition and its sub-types.

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