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Cardiac manifestations of congenital LMNA-related muscular dystrophy in children: three case reports and recommendations for care

Published online by Cambridge University Press:  12 December 2016

Felice Heller ,
Ivana Dabaj ,
Jean K. Mah ,
Jean Bergounioux ,
Aben Essid ,
Carsten G. Bönnemann ,
Anne Rutkowski ,
Gisèle Bonne ,
Susana Quijano-Roy  and
Karim Wahbi
Felice Heller*
Affiliation:
Department of Pediatrics, University of Connecticut School of Medicine, Connecticut Children’s Medical Center, Hartford, Connecticut, United States of America
Ivana Dabaj
Affiliation:
AP-HP, Pediatric Department, Raymond Poincaré Hospital, University Hospitals of West Paris, Garches, France Referral Center for Neuromuscular Diseases Garches-Necker-Mondor-Hendaye (GNMH), French Network of Neuromuscular Diseases (FILNEMUS), Garches, France
Jean K. Mah
Affiliation:
Department of Pediatrics, University of Calgary, Calgary, Alberta, Canada
Jean Bergounioux
Affiliation:
AP-HP, Pediatric Department, Raymond Poincaré Hospital, University Hospitals of West Paris, Garches, France
Aben Essid
Affiliation:
AP-HP, Pediatric Department, Raymond Poincaré Hospital, University Hospitals of West Paris, Garches, France
Carsten G. Bönnemann
Affiliation:
Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, United States of America
Anne Rutkowski
Affiliation:
Cure Congenital Muscular Dystrophy and Kaiser SCPMG, Los Angeles, California, United States of America
Gisèle Bonne
Affiliation:
Sorbonne Universités, UPMC Univ Paris 06, Inserm UMRS974, CNRS FRE3617, Center for Research in Myology, Paris, France Institut de Myologie, Paris, France
Susana Quijano-Roy
Affiliation:
AP-HP, Pediatric Department, Raymond Poincaré Hospital, University Hospitals of West Paris, Garches, France Referral Center for Neuromuscular Diseases Garches-Necker-Mondor-Hendaye (GNMH), French Network of Neuromuscular Diseases (FILNEMUS), Garches, France Versailles-St Quentin University, U1179 UVSQ – INSERM, Montigny, France
Karim Wahbi
Affiliation:
Sorbonne Universités, UPMC Univ Paris 06, Inserm UMRS974, CNRS FRE3617, Center for Research in Myology, Paris, France Institut de Myologie, Paris, France Cardiology Department, AP-HP, Cochin Hospital, Paris Cedex, France AP-HP, Pitié-Salpêtrière Hospital, Referral Center for Muscle Diseases East Paris, Myology Institute, Paris, France Université Paris Descartes-Sorbonne Paris Cité, Paris, France
*
Correspondence to: F. Heller, MD, Division of Pediatric Cardiology, Suite 2B, Connecticut Children’s Medical Center, 282 Washington Street, Hartford, CT 06106, United States of America. Tel: 860 545 9400; Fax: 860 545 9410; E-mail: [email protected]
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Abstract

Skeletal and cardiac muscle laminopathies, caused by mutations in the lamin A/C gene, have a clinical spectrum from congenital LMNA-related muscular dystrophy to later-onset Emery–Dreifuss muscular dystrophy, limb girdle muscular dystrophy, and dilated cardiomyopathy. Although cardiac involvement is observed at all ages, it has only been well described in adults. We present the evolution of cardiac disease in three children with congenital muscular dystrophy presentation of LMNA-related muscular dystrophy. In this series, atrial arrhythmia was the presenting cardiac finding in all three patients. Heart failure developed up to 5 years later. Symptoms of right heart failure, including diarrhoea and peripheral oedema, preceded a rapid decline in left ventricular ejection fraction. Recommendations for cardiac surveillance and management in these patients are made.

Keywords

Lamin A/C LMNAcongenital muscular dystrophycardiomyopathyarrhythmiaautomatic implantable cardiac defibrillator
Type
Original Articles
Information
Cardiology in the Young , Volume 27 , Issue 6 , August 2017 , pp. 1076 - 1082
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Copyright
© Cambridge University Press 2016 

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