Literature DB >> 10909632

[Familial occurrence of Ebstein anomaly].

R Margalit-Stashefski1, A Lorber, E Margalit.   

Abstract

Ebstein anomaly is a rare congenital disease which affects location, structure and mobility of the tricuspid valve, and right atrium and ventricle. Although most cases are sporadic, familial occurrence has been reported. We report 2 brothers born with Ebstein anomaly. The parents were first degree cousins and there were 8 other children. 2 daughters were born with other congenital heart anomalies, 1 with ventricular septal defect and the other with severe pulmonary artery stenosis. We suggest that in some families, Ebstein anomaly is an autosomal dominant disease with different expression in the sexes.

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Mesh:

Year:  1998        PMID: 10909632

Source DB:  PubMed          Journal:  Harefuah        ISSN: 0017-7768


  2 in total

1.  Ebstein's anomaly in siblings: an original observation.

Authors:  Cihangir Uyan; Mehmet Yazici; Ayten Pamukcu Uyan; Ramazan Akdemir; Nejat Imirzalioglu; Barbaros Dokumaci
Journal:  Int J Cardiovasc Imaging       Date:  2002-12       Impact factor: 2.357

2.  Copy number variants in Ebstein anomaly.

Authors:  Andreas Giannakou; Robert J Sicko; Wei Zhang; Paul Romitti; Marilyn L Browne; Michele Caggana; Lawrence C Brody; Laura Jelliffe-Pawlowski; Gary M Shaw; Denise M Kay; James L Mills
Journal:  PLoS One       Date:  2017-12-07       Impact factor: 3.240

  2 in total

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