Abstract
Introduction: Noncompaction cardiomyopathy (NCCM) is a rare disorder in which affected individuals have variable clinical presentations ranging from being asymptomatic to sudden cardiac arrest. While its typical phenotypic expression often triggers the initial evaluation, the etiology is heterogeneous with genetic, familial, or sporadic traits. Treatment and prognosis depends on factors such as the presence or absence of heart failure, cardiac arrhythmia, thromboembolic events, and type of genetic mutation identified.
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