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Article

Cardiomyopathy in Northwestern Mexico: Clinical Spectrum, Morphological Variants, and Sarcomere Gene Mutations.

Archives of medical research - 1 Jun 2026

Machain-Leyva Cyntia Zulema, Arroyo-Rodríguez Cuitláhuac, Padilla-Islas Luis Alejandro, Martínez Hernández Francisco A, Figueroa-Sauceda Sergio Ramón, Zazueta-Armenta Verónica

Abstract excerpt

BACKGROUND: Hypertrophic cardiomyopathy (HCM) is a common genetic heart disease characterized by left ventricular (LV) hypertrophy that cannot be fully explained by abnormal loading conditions. AIM: To describe the clinical spectrum, morphological variants and sarcomere gene mutations in patients with HCM from northwestern Mexico. MATERIALS AND METHODS: We conducted a prospective, cross-sectional study of...

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Identifiers

PMID: 41581477
DOI: 10.1016/j.arcmed.2025.103362

Genes

MYBPC3
MYH7

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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