Literature DB >> 15384079

Monozygotic twins discordant for frontonasal malformation.

Shehla N Mohammed1, Marc C Swan, Steven A Wall, Andrew O M Wilkie.   

Abstract

Frontonasal malformation (FNM), also known as the median cleft face syndrome, encompasses a spectrum of phenotypes that are believed to result from a single underlying aetiology. Over the course of two decades, the Craniofacial Unit at the Radcliffe Infirmary, Oxford has been involved in the management of six same-sex twins where only a single twin is affected. With local ethical committee approval, five sets of twins were traced and consented to participation in this study. Monozygosity of all five twin pairs was confirmed, and the clinical features were reviewed. We discuss the mechanistic relationship between FNM and the twinning process and the genetic implications of this association. (c) 2004 Wiley-Liss, Inc.

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Year:  2004        PMID: 15384079     DOI: 10.1002/ajmg.a.30280

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  3 in total

1.  Frontonasal dysplasia: oral features, restorative and orthodontic dental treatment in a child.

Authors:  R A Valério; C Scatena; F R R Santos; F L Romano; A M Queiroz; F W G Paula-Silva
Journal:  Eur Arch Paediatr Dent       Date:  2017-03-01

2.  Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene.

Authors:  Stephen R F Twigg; Sarah L Versnel; Gudrun Nürnberg; Melissa M Lees; Meenakshi Bhat; Peter Hammond; Raoul C M Hennekam; A Jeannette M Hoogeboom; Jane A Hurst; David Johnson; Alexis A Robinson; Peter J Scambler; Dianne Gerrelli; Peter Nürnberg; Irene M J Mathijssen; Andrew O M Wilkie
Journal:  Am J Hum Genet       Date:  2009-04-30       Impact factor: 11.025

3.  Frontonasal dysplasia: A case report.

Authors:  Se Il Lee; Seung Je Lee; Hong Sil Joo
Journal:  Arch Craniofac Surg       Date:  2019-12-20
  3 in total

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