Phenylketonuria, Maternal
A condition occurring in untreated or partially treated females with PHENYLKETONURIA when they become pregnant. This may result in damages to the FETUS, including MICROCEPHALY; MENTAL RETARDATION; congenital heart disease; FETAL GROWTH RETARDATION; and CRANIOFACIAL ABNORMALITIES. (From Am J Med Genet 1997 Mar 3;69(1):89-95)
Year introduced: 1992
PubMed search builder options
Subheadings:
Tree Number(s): C10.228.140.163.100.687.500, C12.050.703.575, C16.320.565.100.766.500, C16.320.565.189.687.500, C18.452.132.100.687.500, C18.452.648.100.766.500, C18.452.648.189.687.500
MeSH Unique ID: D017042
Entry Terms:
- Maternal Phenylketonuria
- Phenylalanine-Hydroxylase Deficiency Disease, Maternal
- Phenylalanine Hydroxylase Deficiency Disease, Maternal
- PKU, Maternal
- Maternal Phenylalanine Hydroxylase Deficiency Disease
- Pregnancy in Phenylketonuria
- Phenylketonuria, Pregnancy in
Previous Indexing:
See Also: