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Hypertrophic Cardiomyopathy in the Elderly: A Case Identified With Genetic Screening

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Abstract

Hypertrophic cardiomyopathy (HCM) is a hereditary disease with an autosomal dominant pattern of inheritance, that is caused by a mutation in one of several sarcomere genes that encodes components of the contractile system of the heart. Hypertrophic cardiomyopathy has been described as a disease that is more heavily diagnosed in the second decade of life, that may present with abnormal syncopal episodes or sudden cardiac death. However, with a better understanding of the genetic changes that occur in HCM and with improved imaging techniques, there has now been an increased recognition of a late-onset disease that can occur in the elderly population. We report a case of a 73-year-old woman who was found to have HCM after various clinical events took place.

References
1.
Tower-Rader A, Mohananey D, To A, Lever H, Popovic Z, Desai M . Prognostic Value of Global Longitudinal Strain in Hypertrophic Cardiomyopathy: A Systematic Review of Existing Literature. JACC Cardiovasc Imaging. 2018; 12(10):1930-1942. DOI: 10.1016/j.jcmg.2018.07.016. View

2.
Lee D, Rakowski H . Hypertrophic Cardiomyopathy in Elderly Individuals: Is It a Rose by Another Name?. J Am Heart Assoc. 2021; 10(3):e020204. PMC: 7955421. DOI: 10.1161/JAHA.120.020204. View

3.
Maron B, Maron M, Semsarian C . Genetics of hypertrophic cardiomyopathy after 20 years: clinical perspectives. J Am Coll Cardiol. 2012; 60(8):705-15. DOI: 10.1016/j.jacc.2012.02.068. View

4.
Wolf C . Hypertrophic cardiomyopathy: genetics and clinical perspectives. Cardiovasc Diagn Ther. 2019; 9(Suppl 2):S388-S415. PMC: 6837941. DOI: 10.21037/cdt.2019.02.01. View

5.
Iung B, Baron G, Butchart E, Delahaye F, Gohlke-Barwolf C, Levang O . A prospective survey of patients with valvular heart disease in Europe: The Euro Heart Survey on Valvular Heart Disease. Eur Heart J. 2003; 24(13):1231-43. DOI: 10.1016/s0195-668x(03)00201-x. View