Familial cardiac laminopathy with predominant atrial involvement: a case series of a family with <i>LMNA</i> mutation
The familial occurrence of atrial arrhythmias without significant ventricular involvement in several family members with heterozygous <i>LMNA</i> missense mutation underscores the potential genetic component in cardiac arrhythmias, especially if arrhythmias occur in younger individuals without common risk factors.
Authors
- Jocelyn Inamo (ORCID: https://orcid.org/0000-0002-1057-9699)
- Véronique Fressart (ORCID: https://orcid.org/0000-0003-4749-1428)
- Romain Vergier (ORCID: https://orcid.org/0009-0001-2450-9595)
- Astrid Monfort (ORCID: https://orcid.org/0000-0002-4432-5566)
- Andréas Müssigbrodt (ORCID: https://orcid.org/0000-0003-0748-0302)
- Patrice Bouvagnet (ORCID: https://orcid.org/0000-0001-7583-0533)
- Pascale Richard (ORCID: https://orcid.org/0000-0002-2390-3005)
- Maria Herrera Bethencourt (ORCID: https://orcid.org/0009-0004-5665-5759)
Institutions
- Sorbonne Université (FR)
- Assistance Publique – Hôpitaux de Paris (FR)
- Centre Hospitalier Universitaire de Martinique (MQ)
Publication Details
- Journal
- European Heart Journal - Case Reports
- Published
- 2025-03-14
- DOI
- https://doi.org/10.1093/ehjcr/ytaf129
- Primary Topic
- Cardiomyopathy and Myosin Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00