A novel GJA1 mutation causing familial oculodentodigital dysplasia with dilated cardiomyopathy and arrhythmia

Carol A Wittlieb-Weber; Katrina M Haude; Chin-To Fong; Jeffrey M Vinocur

doi:10.1016/j.hrcr.2015.08.013

A novel GJA1 mutation causing familial oculodentodigital dysplasia with dilated cardiomyopathy and arrhythmia

HeartRhythm Case Rep. 2015 Oct 13;2(1):32-35. doi: 10.1016/j.hrcr.2015.08.013. eCollection 2016 Jan.

Authors

Carol A Wittlieb-Weber¹, Katrina M Haude², Chin-To Fong², Jeffrey M Vinocur¹

Affiliations

¹ University of Rochester School of Medicine and Dentistry, Department of Pediatrics, Division of Pediatric Cardiology.
² University of Rochester School of Medicine and Dentistry, Department of Pediatrics, Division of Genetics, Rochester, New York.

No abstract available

Keywords: Cx43, connexin 43; Dilated cardiomyopathy; Heart block; Heart failure; ODDD, Oculodentodigital dysplasia; Oculodentodigital dysplasia; Pediatrics; RBBB, right bundle branch block.

Publication types

Case Reports