Neuromuscular Disorders
Volume 20, Issue 8 , Pages 479-492, August 2010

Hereditary muscular dystrophies and the heart

  • M.C.E. Hermans

      Affiliations

    • Department of Neurology, Maastricht University Medical Centre, P.O. Box 5800, 6202 AZ, Maastricht, The Netherlands
    • Corresponding Author InformationCorresponding author. Tel.: +31 43 3877059; fax: +31 43 3877055.
  • ,
  • Y.M. Pinto

      Affiliations

    • Department of Cardiology, Academic Medical Centre Amsterdam, The Netherlands
  • ,
  • I.S.J. Merkies

      Affiliations

    • Department of Neurology, Maastricht University Medical Centre, P.O. Box 5800, 6202 AZ, Maastricht, The Netherlands
    • Department of Neurology, Spaarne Hospital, Hoofddorp, The Netherlands
  • ,
  • C.E.M. de Die-Smulders

      Affiliations

    • Department of Clinical Genetics, Maastricht University Medical Centre, Maastricht, The Netherlands
  • ,
  • H.J.G.M. Crijns

      Affiliations

    • Department of Cardiology, Maastricht University Medical Centre, Maastricht, The Netherlands
  • ,
  • C.G. Faber

      Affiliations

    • Department of Neurology, Maastricht University Medical Centre, P.O. Box 5800, 6202 AZ, Maastricht, The Netherlands

Received 5 January 2010; received in revised form 19 April 2010; accepted 21 April 2010.

Summary 

Cardiac disease is a common clinical manifestation of neuromuscular disorders, particularly of muscular dystrophies. Heart muscle cells as well as specialized conducting myocardial fibres may be affected by the dystrophic process. The incidence and nature of cardiac involvement vary with different types of muscular dystrophies. Some mainly lead to myocardial disease, resulting in cardiomyopathy and heart failure, while others particularly affect the conduction system, leading to arrhythmias and sudden death. As prognosis of muscular dystrophy patients may be directly related to cardiac status, surveillance and timely management of cardiac complications are important. However, recognition of cardiac involvement requires active investigation and remains challenging since typical signs and symptoms of cardiac dysfunction may not be present and progression is unpredictable.

In this review, we present a comprehensive overview of hereditary muscular dystrophies associated with cardiac disease to provide an efficient strategy for the expertise and management of these diseases.

Keywords: Muscular dystrophy, Cardiomyopathy, Arrhythmia, Sudden death, Treatment

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0960-8966(10)00189-6

doi:10.1016/j.nmd.2010.04.008

Neuromuscular Disorders
Volume 20, Issue 8 , Pages 479-492, August 2010