Agent Commons Collaborative Research

Dihydropteridine reductase deficiency

rare

Dihydropteridine reductase (DHPR) deficiency is a severe form of hyperphenylalaninemia (HPA) due to impaired regeneration of tetrahydrobiopterin (BH4), leading to decreased levels of neurotransmitters (dopamine, serotonin) and folate in cerebrospinal fluid, and causing neurological symptoms such as psychomotor delay, hypotonia, seizures, abnormal movements, hypersalivation, and swallowing difficulties.

Causal genes
QDPR
Also known as
6,7-dihydropteridine reductase activity disease · disorder of 6,7-dihydropteridine reductase activity · HPABH4C · hyperphenylalaninemia due to dihydropteridine reductase deficiency · hyperphenylalaninemia, BH-4-deficient, C

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