Literature DB >> 11999984

Nasomaxillary hypoplasia and severe orofacial clefting in a child of a mother with phenylketonuria.

E Sweeney1, A Fryer.   

Abstract

The offspring of mothers with untreated or poorly controlled phenylketonuria (PKU) (McKusick 261600) are at risk of having congenital anomalies including microcephaly, congenital heart defects and developmental delay (Rouse et al 1997). We report a child born to a mother with poorly controlled PKU and suggest that the facial abnormalities seen in this child could be part of the specturn of maternal PKU embryopathy.

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Year:  2002        PMID: 11999984     DOI: 10.1023/a:1015102320233

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  3 in total

1.  Lobar holoprosencephaly in an infant born to a mother with classic phenylketonuria.

Authors:  K Keller; H McCune; C Williams; M Muenke
Journal:  Am J Med Genet       Date:  2000-11-13

2.  Maternal Phenylketonuria Collaborative Study (MPKUCS) offspring: facial anomalies, malformations, and early neurological sequelae.

Authors:  B Rouse; C Azen; R Koch; R Matalon; W Hanley; F de la Cruz; F Trefz; E Friedman; H Shifrin
Journal:  Am J Med Genet       Date:  1997-03-03

3.  Maternal phenylketonuria: magnetic resonance imaging of the brain in offspring.

Authors:  H L Levy; D Lobbregt; P D Barnes; T Y Poussaint
Journal:  J Pediatr       Date:  1996-06       Impact factor: 4.406

  3 in total
  1 in total

1.  Cardiac teratogenicity in mouse maternal phenylketonuria: defining phenotype parameters and genetic background influences.

Authors:  Nikki J Seagraves; Kim L McBride
Journal:  Mol Genet Metab       Date:  2012-08-08       Impact factor: 4.797

  1 in total

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