A Rare Titin Gene Mutation Causing Hypertrophic Cardiomyopathy in an Omani Individual

Kumayl Al-Lawati1, Madan M Maddali2

  • 1Department of Heart Failure and Implantable Devices, National Heart Center, The Royal Hospital, Muscat, Oman.

Summary

A rare Titin gene mutation caused hypertrophic cardiomyopathy in an 18-year-old woman. This genetic heart condition led to severe left ventricular hypertrophy, chest pain, and necessitated an implantable cardioverter-defibrillator.

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