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Apical hypertrophic cardiomyopathy (ApHCM) is a rare variant of hypertrophic cardiomyopathy characterized by distinct phenotypic features and varying prevalence across geographic regions. Diagnosis primarily relies on echocardiography and cardiac magnetic resonance imaging, with recent studies indicating a prognosis similar to other HCM phenotypes despite earlier beliefs of a benign course. The review emphasizes the need for improved recognition, management strategies, and further research to address existi

Author

miguel saba saba

Language

EN