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Left ventricular non-compaction cardiomyopathy: restrictive subtype with MYH7 gene mutation

Published online by Cambridge University Press:  11 October 2022

Kazim Oztarhan Open the ORCID record for Kazim Oztarhan [Opens in a new window] ,
Beyza Senturk  and
Ozlem Ucar
Kazim Oztarhan*
Affiliation:
Department of Pediatric Cardiology, T.C. Demiroglu Bilim University, Istanbul, Turkey
Beyza Senturk
Affiliation:
Department of Pediatrics, T.C. Demiroglu Bilim University, Istanbul, Turkey
Ozlem Ucar
Affiliation:
Department of Pediatrics, T.C. Demiroglu Bilim University, Istanbul, Turkey
*
Author for correspondence: Kazim Oztarhan, Esentepe, Buyukdere St. No:120 34394, Sisli/Istanbul, Turkey. Tel: +90 (532) 357 87 50. E-mail: oztarhank@gmail.com
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Abstract

Left ventricular non-compaction is a very rare, still unclassified congenital cardiomyopathy. Nine distinct subtypes of functional and anatomical left ventricular non-compaction have been identified. Studies on the prognosis and mortality of subtypes are ongoing. Our study presented the first restrictive subtype left ventricular non-compaction case with family history and MYH7 gene mutation.

Keywords

Left ventricular non-compactionrestrictive cardiomyopathyMYH7 gene
Type
Brief Report
Information
Cardiology in the Young , Volume 33 , Issue 5 , May 2023 , pp. 810 - 812
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Copyright
© The Author(s), 2022. Published by Cambridge University Press

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