Literature DB >> 16681404

Pierre Robin sequence with esophageal atresia and congenital radioulnar synostosis.

Keramettin Ugur Ozkan1, Yusuf Kenan Coban, Murat Uzel, Mehmet Ergun, Hafize Oksuz.   

Abstract

A wide spectrum of anomalies can be associated with Pierre Robin sequence. This report presents a 3-day-old infant with micrognathia, U-shaped cleft palate, low-set right ear with microtia, glossoptosis, esophageal atresia, and right congenital radioulnar synostosis. The association of congenital radioulnar synostosis and esophageal atresia with Pierre Robin sequence has not been previously described.

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Year:  2006        PMID: 16681404     DOI: 10.1597/05-032.1

Source DB:  PubMed          Journal:  Cleft Palate Craniofac J        ISSN: 1055-6656


  4 in total

1.  Cervico-thoracic kyphosis in a girl with Pierre Robin sequence.

Authors:  Ali Al Kaissi; Rudolf Ganger; Klaus Klaushofer; Franz Grill
Journal:  Ger Med Sci       Date:  2011-03-14

2.  BMPR1B mutation causes Pierre Robin sequence.

Authors:  Yongjia Yang; Jianying Yuan; Xu Yao; Rong Zhang; Hui Yang; Rui Zhao; Jihong Guo; Ke Jin; Haibo Mei; Yongqi Luo; Liu Zhao; Ming Tu; Yimin Zhu
Journal:  Oncotarget       Date:  2017-04-18

3.  Prenatal features of mandibulofacial dysostosis Guion-Almeida Type.

Authors:  Vlad Dragoi; Florina Nedelea; Nicolae Gica; Radu Botezatu; Gheorghe Peltecu; Anca Maria Panaitescu
Journal:  J Med Life       Date:  2021 Sep-Oct

4.  Pierre Robin sequence: Subdivision, data, theories, and treatment - Part 1: History, subdivisions, and data.

Authors:  Kurt-W Bütow; Roger Arthur Zwahlen; Jean A Morkel; Sharan Naidoo
Journal:  Ann Maxillofac Surg       Date:  2016 Jan-Jun
  4 in total

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