Literature DB >> 2260599

Congenital heart disease and Robinow syndrome: coincidence or an additional component of the syndrome?

S A Webber1, D S Wargowski, D Chitayat, G G Sandor.   

Abstract

We report on a girl with Robinow syndrome and pulmonary atresia with ventricular septal defect (VSD). Seven cases of Robinow syndrome with congenital heart defect (CHD) have now been described, 5 of whom had stenosis or atresia of the pulmonic valve. This suggests that CHD, especially right ventricular outlow obstruction, may be a component manifestation of this syndrome in some cases. Since early recognition of this type of heart lesion can minimize morbidity by facilitating optimal surgical therapy, thorough cardiac evaluation of all patients with Robinow syndrome seems warranted.

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Year:  1990        PMID: 2260599     DOI: 10.1002/ajmg.1320370418

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  6 in total

Review 1.  Robinow syndrome.

Authors:  M A Patton; A R Afzal
Journal:  J Med Genet       Date:  2002-05       Impact factor: 6.318

2.  Robinow syndrome in two siblings from consanguineous parents.

Authors:  D F Schorderet; S Dahoun; I Defrance; D Nusslé; M A Morris
Journal:  Eur J Pediatr       Date:  1992-08       Impact factor: 3.183

3.  Unusual traits associated with Robinow syndrome.

Authors:  M A Sabry; E A Ismail; R L al-Naggar; N A al-Torki; S Farah; S A al-Awadi; D Obenbergerova; L Bastaki
Journal:  J Med Genet       Date:  1997-09       Impact factor: 6.318

4.  Robinow Syndrome: A Rare Case Report and Review of Literature.

Authors:  Cristalle Soman; Ashok Lingappa
Journal:  Int J Clin Pediatr Dent       Date:  2015-08-11

5.  Variants in the Regulatory Region of WNT5A Reduced Risk of Cardiac Conotruncal Malformations in the Chinese Population.

Authors:  Peiqiang Li; Haijie Li; Yufang Zheng; Bin Qiao; Wenyuan Duan; Lijuan Huang; Weiqi Liu; Hongyan Wang
Journal:  Sci Rep       Date:  2015-08-17       Impact factor: 4.379

6.  Prickle1 mutation causes planar cell polarity and directional cell migration defects associated with cardiac outflow tract anomalies and other structural birth defects.

Authors:  Brian C Gibbs; Rama Rao Damerla; Eszter K Vladar; Bishwanath Chatterjee; Yong Wan; Xiaoqin Liu; Cheng Cui; George C Gabriel; Maliha Zahid; Hisato Yagi; Heather L Szabo-Rogers; Kaye L Suyama; Jeffrey D Axelrod; Cecilia W Lo
Journal:  Biol Open       Date:  2016-02-16       Impact factor: 2.422

  6 in total

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