Last update 01 Nov 2024

Hyperphenylalaninemia, BH4-Deficient, B

Basic Info

Synonyms
GTP - Guanosine-5-triphosphate cyclohydrolase deficiency, GTP CYCLOHYDROLASE I DEFICIENCY, GTP Cyclohydrolase I Deficiency
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Introduction
An autosomal recessive condition caused by mutation(s) in the GCH1 gene, encoding GTP cyclohydrolase 1. It is characterized by hyperphenylalaninemia and GTP cyclohydrolase 1-deficient dopa-responsive dystonia.

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