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Article

Heterozygous desmin gene (DES) mutation contributes to familial dilated cardiomyopathy.

The Journal of international medical research - 1 Apr 2021

Huang Ying-Shuo, Xing Yun-Li, Li Hong-Wei

Abstract excerpt

Familial dilated cardiomyopathy (FDCM) is characterized by high genetic heterogeneity and an increased risk of heart failure or sudden cardiac death in adults. We report the case of a 62-year-old man with a 2-month history of shortness of breath during activity, without paroxysmal nocturnal dyspnea. The patient underwent a series of examinations including transthoracic echocardiography, coronary arteriography,...

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Aged
Cardiomyopathy and Myosin Studies
Cardiomyopathy, Dilated
Desmin
Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Ventricular Function, Left

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Identifiers

PMID: 33823640
DOI: 10.1177/03000605211006598
PMCID: PMC8033466

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

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