Lamin A/C cardiomyopathy: young onset, high penetrance, and frequent need for heart transplantation

Author:

Hasselberg Nina Eide123,Haland Trine Fink123,Saberniak Jørg123,Brekke Pål Haugar1,Berge Knut Erik4,Leren Trond Paul4,Edvardsen Thor123,Haugaa Kristina Hermann123

Affiliation:

1. Department of Cardiology, Center for Cardiological Innovation, Oslo University Hospital, Rikshospitalet, PO Box 4950 Nydalen, 0424 Oslo, Norway

2. Faculty of Medicine, Institute of Clinical Medicine, University of Oslo, Rikshospitalet, PO Box 4950, 0424 Oslo, Norway

3. Institute for Surgical Research, Oslo University Hospital, Rikshospitalet, PO Box 4950 Nydalen, 0424 Oslo, Norway

4. Unit for Cardiac and Cardiovascular Genetics, Department of Medical Genetics, Oslo University Hospital, Ullevål, PO Box 4956 Nydalen, 0424 Oslo, Norway

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

Reference15 articles.

1. Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers;van Rijsingen;Eur J Heart Fail,2013

2. Risk prediction of ventricular arrhythmias and myocardial function in lamin A/C mutation positive subjects;Hasselberg;Europace,2014

3. Mechanical dispersion by strain echocardiography: a predictor of ventricular arrhythmias in subjects with lamin A/C mutations;Haugaa;JACC Cardiovasc Imaging,2015

4. 2015 ESC guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: the task force for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death of the European Society of Cardiology (ESC). Endorsed by: Association for European Paediatric and Congenital Cardiology (AEPC);Priori;Eur Heart J,2015

5. Meta-analysis of clinical characteristics of 299 carriers of LMNA gene mutations: do lamin A/C mutations portend a high risk of sudden death?;van Berlo;J Mol Med (Berl),2005

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