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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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References

Singh, DP, Patel, H. Left Ventricular Non-compaction Cardiomyopathy. StatPearls Publishing,, Treasure Island (FL), 2021.Google Scholar
Phan, HT. Non-compaction cardiomyopathy misdiagnosed as dilated cardiomyopathy. J Case Rep 2018; 8: 1–13.Google Scholar
Towbin, JA, Jefferies, JL. Cardiomyopathies due to left ventricular noncompaction, mitochondrial and storage diseases, and inborn errors of metabolism. Circ Res 2017; 121: 7–854.Google ScholarPubMed
Mehaney, DA, Haghighi, A, Embaby, AK, et al. Molecular analysis of dilated and left ventricular noncompaction cardiomyopathies in Egyptian children. Cardiol Young 2022; 32: 2–300.CrossRefGoogle ScholarPubMed
Jefferies, JL. Left ventricular noncompaction cardiomyopathy: new clues in a not so new disease? J Am Heart Assoc 2021; 10: 2.CrossRefGoogle Scholar
Suvarna, JC, Deshmukh, CT, Hajela, SA. Left ventricular noncompaction: a cardiomyopathy often mistaken. Indian J Med Sci 2009; 63: 7–307.CrossRefGoogle ScholarPubMed
Vaidya, VR, Lyle, M, Miranda, WR, et al. Long-term survival of patients with left ventricular noncompaction. J Am Heart Assoc 2021; 10: 2.CrossRefGoogle ScholarPubMed
van Waning, JI, Caliskan, K, Hoedemaekers, YM, et al. Genetics, clinical features, and long-term outcome of noncompaction cardiomyopathy. J Am Coll Cardiol 2018; 71: 7–722.CrossRefGoogle ScholarPubMed
Miszalski-Jamka, K, Jefferies, JL, Mazur, W, et al. Novel genetic triggers and genotype-phenotype correlations in patients with left ventricular noncompaction. Circulation: Cardiovasc Genet 2017; 10: 4.Google ScholarPubMed
Patil, VC, Patil, HV. Isolated non-compaction cardiomyopathy presented with ventricular tachycardia. Heart Views: Off J Gulf Heart Assoc 2011; 12: 2.CrossRefGoogle ScholarPubMed