Clinical Research in Cardiology

, Volume 100, Issue 7, pp 627–628 | Cite as

A case of familial hypertrophic cardiomyopathy emphasizes the importance of parallel screening of multiple disease genes

  • Thomas Scheffold
  • Stephan Waldmüller
  • Konstantin Borisov
Letter to the Editors

Notes

Acknowledgments

This work was in part supported by the Adolf-Schilling-Stiftung Münster. We thank also Mrs. Joanne Davis for technical help and revising the manuscript.

References

  1. 1.
    Arad M, Maron BJ et al (2005) Glycogen storage diseases presenting as hypertrophic cardiomyopathy. N Engl J Med 352(4):362–372PubMedCrossRefGoogle Scholar
  2. 2.
    Gollob MH, Green MS et al (2001) Identification of a gene responsible for familial Wolff-Parkinson-White syndrome. N Engl J Med 344(24):1823–1831PubMedCrossRefGoogle Scholar
  3. 3.
    Ingles J, Doolan A et al (2005) Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling. J Med Genet 42(10):e59PubMedCrossRefGoogle Scholar

Copyright information

© Springer-Verlag 2011

Authors and Affiliations

  • Thomas Scheffold
    • 1
  • Stephan Waldmüller
    • 2
  • Konstantin Borisov
    • 3
  1. 1.Department Biobank/KardiogenetikInstitut Für Herzinfarktforschung Ludwigshafen an der Universität HeidelbergLudwigshafen/RheinGermany
  2. 2.Institut für HerzkreislaufforschungUniversität Witten/HerdeckeDortmundGermany
  3. 3.Department of Cardiology and SurgeryRehabilitation Center of the Executive Office of the President of Russian FederationMoscowRussia

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