Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies: Results From a Dutch Multicenter Cohort Study.

doi:10.1016/j.jchf.2023.07.007

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Article

Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies: Results From a Dutch Multicenter Cohort Study.

JACC. Heart failure - 1 Jan 2024

Jansen Mark, de Brouwer Remco, Hassanzada Fahima, Schoemaker Angela E, Schmidt Amand F, Kooijman-Reumerman Maria D, Bracun Valentina, Slieker Martijn G, Dooijes Dennis, Vermeer Alexa M C, Wilde Arthur A M, Amin Ahmad S, Lekanne Deprez Ronald H, Herkert Johanna C, Christiaans Imke, de Boer Rudolf A, Jongbloed Jan D H, van Tintelen J Peter, Asselbergs Folkert W, Baas Annette F

Abstract excerpt

BACKGROUND: MYH7 variants cause hypertrophic cardiomyopathy (HCM), noncompaction cardiomyopathy (NCCM), and dilated cardiomyopathy (DCM). Screening of relatives of patients with genetic cardiomyopathy is recommended from 10 to 12 years of age onward, irrespective of the affected gene. OBJECTIVES: This study sought to study the penetrance and prognosis of MYH7 variant-associated cardiomyopathies. METHODS: In this...

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PMID: 37565978
DOI: 10.1016/j.jchf.2023.07.007

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