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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
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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

Information

Type
Brief Report
Information
Cardiology in the Young , Volume 32 , Issue 4 , April 2022 , pp. 674 - 675
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Copyright
© The Author(s), 2021. Published by Cambridge University Press

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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

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