Literature DB >> 10203668

Undiagnosed maternal phenylketonuria: the need for prenatal selective screening or case finding.

W B Hanley1, L D Platt, R P Bachman, N Buist, M T Geraghty, J Isaacs, M E O'Flynn, W J Rhead, G Seidlitz, B Tishler.   

Abstract

OBJECTIVES: The aims of this article are to report on a review of cases of maternal phenylketonuria in the International Maternal Phenylketonuria Collaborative Study that were initially diagnosed during or after a pregnancy, to alert health care practitioners to the possible existence of women with undiagnosed phenylketonuria whose fetuses are at risk, and to emphasize that not all adults with untreated phenylketonuria are mentally retarded. STUDY
DESIGN: The study was conducted through retrospective database review.
RESULTS: Of 414 women with live-born infants, 17 fulfilled our criteria. Six had phenylketonuria diagnosed after they had produced >/=1 affected offspring, 2 had phenylketonuria diagnosed as a result of transient postnatal hyperphenylalaninemia in an offspring, and 9 had phenylketonuria diagnosed by prenatal screening. Undiagnosed maternal phenylketonuria in North America and Europe is currently estimated at 1 case/100,000 births; this rate could be higher elsewhere.
CONCLUSIONS: Physicians and midwives should consider a protocol of selective prenatal screening or case finding to detect undiagnosed phenylketonuria among their patients.

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Year:  1999        PMID: 10203668     DOI: 10.1016/s0002-9378(99)70671-x

Source DB:  PubMed          Journal:  Am J Obstet Gynecol        ISSN: 0002-9378            Impact factor:   8.661


  3 in total

1.  Maternal phenylketonuria: the French survey.

Authors:  François Feillet; Véronique Abadie; Jacques Berthelot; Nicole Maurin; Hélène Ogier; Michel Vidailhet; Jean-Pierre Farriaux; Loic de Parscau
Journal:  Eur J Pediatr       Date:  2004-07-06       Impact factor: 3.183

2.  Large neutral amino acid supplementation increases melatonin synthesis in phenylketonuria: a new biomarker.

Authors:  Shoji Yano; Kathryn Moseley; Colleen Azen
Journal:  J Pediatr       Date:  2012-11-16       Impact factor: 4.406

3.  An exceptional Albanian family with seven children presenting with dysmorphic features and mental retardation: maternal phenylketonuria.

Authors:  Ina Knerr; Johannes Zschocke; Stefan Schellmoser; Hans G Topf; Corina Weigel; Jörg Dötsch; Wolfgang Rascher
Journal:  BMC Pediatr       Date:  2005-04-05       Impact factor: 2.125

  3 in total

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