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Maternal phenylketonuria
rareA disorder of development or morphogenesis characterized by the development of microcephaly, growth retardation, congenital heart disease, facial dysmorphism and intellectual disability in nonphenylketonuric offspring of mothers with excess phenylalanine (Phe) concentrations.
- Identifiers
- MONDO:0016366 Orphanet:2209
- Also known as
- hyperphenylalaninemic embryopathy · maternal hyperphenylalaninemia · maternal PKU syndrome · phenylketonuric embryopathy
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