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Article

Familial dilated cardiomyopathy caused by a novel variant in the Lamin A/C gene: a case report.

BMC cardiovascular disorders - 22 Sept 2020

Huang Jing, Wan Qing, Zou Yu, Wang Lijie, Pan Yesheng

Abstract excerpt

BACKGROUND: Familial dilated cardiomyopathy (FDCM) is most commonly inherited as an autosomal dominant trait. The Lamin A/C (LMNA) gene variants have been identified to be associated with DCM, conductive system disorders, type 2 Emery-Dreifuss muscular dystrophy and several other disorders. Here, we reported a novel variant in the LMNA gene that might be related to FDCM. CASE PRESENTATION: A 30-year-old young man...

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Share to Arrhythmias, Cardiac
Share to Cardiomyopathy, Dilated
Share to Catheter Ablation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Predisposition to Disease

Share to Heterozygote

Share to Lamin Type A

Share to Mutation, Missense

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Source

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Identifiers

PMID: 32962641
DOI: 10.1186/s12872-020-01695-8
PMCID: PMC7509919

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

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