Hostname: page-component-78c5997874-lj6df Total loading time: 0 Render date: 2024-11-17T23:04:07.407Z Has data issue: false hasContentIssue false
  • English
  • Français

Case Report of a 33-year-old with Ebstein malformation of tricuspid valve and hypertrophic cardiomyopathy

Part of: Cardiac Morphology

Published online by Cambridge University Press:  09 September 2021

Sedigheh Saedi Open the ORCID record for Sedigheh Saedi [Opens in a new window] ,
Pooneh Pashapour  and
Golnaz Houshmand
Sedigheh Saedi*
Affiliation:
Rajaie Cardiovascular Medical and Research Center, Tehran, Iran
Pooneh Pashapour
Affiliation:
Rajaie Cardiovascular Medical and Research Center, Tehran, Iran
Golnaz Houshmand
Affiliation:
Rajaie Cardiovascular Medical and Research Center, Tehran, Iran
*
Author for correspondence: S. Saedi, Rajaie Cardiovascular Medical and Research Center, Tehran, Iran. Tel: 00982123921. E-mail: sedsaedi@gmail.com
Get access Rights & Permissions [Opens in a new window]

Abstract

Ebstein malformation of tricuspid valve is a congenital disease of tricuspid valve with associated right ventricular cardiomyopathy. Hypertrophic cardiomyopathy is a form of inherited left ventricular cardiomyopathy caused by sarcomeric protein gene mutations with inherent risks of sudden cardiac death. Here we report a rare case with co-occurrence of Ebstein malformation of tricuspid valve and hypertrophic cardiomyopathy in a young patient.

Keywords

Ebstein malformation of tricuspid valvehypertrophic cardiomyopathyCHD
Type
Brief Report
Information
Cardiology in the Young , Volume 32 , Issue 4 , April 2022 , pp. 674 - 675
Check for updates
Copyright
© The Author(s), 2021. Published by Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Attenhofer Jost, CH, Connolly, HM, Dearani, JA, Edwards, WD, Danielson, GK. Ebstein’s anomaly. Circulation 2007; 115: 277–285.10.1161/CIRCULATIONAHA.106.619338CrossRefGoogle ScholarPubMed
McGee, M, Warner, L, Collins, N. Ebstein’s anomaly, left ventricular noncompaction, and sudden cardiac death. Case Rep Cardiol 2015; 2015: 854236.Google ScholarPubMed
van Engelen, K, Postma, AV, Van De Meerakker, JB, et al. Ebstein’s anomaly may be caused by mutations in the sarcomere protein gene MYH7. Neth Heart J 2013; 21: 113–117.10.1007/s12471-011-0141-1CrossRefGoogle ScholarPubMed
Maron, BJ, Maron, MS, Olivotto, I. Hypertrophic Cardiomyopathy in Braunwald’s Heart Disease: A Textbook of Cardiovascular Medicine. 11th edn. Elsevier, Philadelphia, PA, 2019.Google Scholar
Saedi, S, Oraii, S, Hajsheikholeslami, F. A cross sectional study on prevalence and etiology of syncope in Tehran. Acta Med Iran 2013; 51: 715–719.Google ScholarPubMed
de Agustín, JA, de Isla, LP, Zamorano, JL. Ebstein anomaly and hypertrophic cardiomyopathy. Eur Heart J 2008; 29: 2525. DOI 10.1093/eurheartj/ehn186.CrossRefGoogle ScholarPubMed
Lee, WC, Fu, M, Fang, HY. Unusual combination: Ebstein’s anomaly and hypertrophic obstructive cardiomyopathy. J Echocardiogr 2016; 14: 42–44.10.1007/s12574-016-0273-9CrossRefGoogle ScholarPubMed

Saedi et al. supplementary material

Saedi et al. supplementary material

Download Saedi et al. supplementary material(Video)
Video 1.5 MB

Saedi et al. supplementary material

Saedi et al. supplementary material 2

Download Saedi et al. supplementary material(Video)
Video 573.4 KB