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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
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

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