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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)
推出的年份: 1992
副标题
树号: 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 单一 ID: D017042
进入的组:
  • 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
早前的内容:
  • Phenylketonuria (1966-1991)

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