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Dihydropteridine reductase deficiency
rareDihydropteridine 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.
- Identifiers
- MONDO:0009862 OMIM:261630Orphanet:226
- Causal genes
- QDPR
- Part of
- Hyperphenylalaninemia due to tetrahydrobiopterin deficiencyTetrahydrobiopterin metabolic process disease
- 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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