Literature DB >> 11158484

American Academy of Pediatrics: Maternal phenylketonuria.

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Abstract

Elevated maternal phenylalanine levels during pregnancy are teratogenic and may result in growth retardation, significant psychomotor handicaps, and birth defects in the offspring of unmonitored and untreated pregnancies. Women of childbearing age with all forms of phenylketonuria, including mild variants such as hyperphenylalaninemia, should receive counseling concerning their risks for adverse fetal effects optimally before conceiving. The best outcomes occur when strict control of maternal phenylalanine levels is achieved before conception and continued throughout the pregnancy.

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Year:  2001        PMID: 11158484     DOI: 10.1542/peds.107.2.427

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  3 in total

1.  Phenylketonuria: an inborn error of phenylalanine metabolism.

Authors:  Robin A Williams; Cyril D S Mamotte; John R Burnett
Journal:  Clin Biochem Rev       Date:  2008-02

2.  Effects and clinical significance of tetrahydrobiopterin supplementation in phenylalanine hydroxylase-deficient hyperphenylalaninaemia.

Authors:  G Gramer; P Burgard; S F Garbade; M Lindner
Journal:  J Inherit Metab Dis       Date:  2007-08-06       Impact factor: 4.982

Review 3.  Contraceptive use in women with inherited metabolic disorders: a retrospective study and literature review.

Authors:  Jessica I Gold; Nina B Gold; Diva D DeLeon; Rebecca Ganetzky
Journal:  Orphanet J Rare Dis       Date:  2022-02-08       Impact factor: 4.123

  3 in total

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