Mitochondrial Cardiomyopathy

AC Blank, JMPJ Breur, S.A. Fuchs, K Koop, AF Baas

Research output: Chapter in Book/Report/Conference proceedingChapterAcademic

Abstract

This thoroughly revised third edition provides a comprehensive grounding on hereditary heart diseases with special emphasis on the genetic aspects of these conditions. It continues to provide the expertise that all cardiologists, clinical and molecular geneticists, and related medical professionals require to provide optimal care for patients with cardiac disease of genetic origin and for their relatives. Topics covered include the different cardiomyopathies, the primary arrhythmia syndromes and the hereditary thoracic aortic disorders. In addition other topics such as cardiac involvement in hereditary neuromuscular diseases, the clinical policy for sudden cardiac death and the possibilities of pre-implantation genetic diagnosis are included to extend the discussion. Clinical Cardiogenetics compiles current knowledge on the topic in an easy to understand reference. It provides a practical clinical primer for cardiologists, clinical geneticists, trainees and other physicians involved in the management of these patients.

Original languageEnglish
Title of host publicationClinical Cardiogenetics
Subtitle of host publicationMitochondrial cardiomyopathy
EditorsHubert Baars, P.A.F.M. Doevendans, Arjan Houweling, Peter van Tintelen
PublisherSpringer
Chapter11
Pages179-190
Edition3
ISBN (Electronic)978-3-030-45457-9
ISBN (Print)978-3-030-45456-2
DOIs
Publication statusPublished - 2020

Keywords

  • Brugada syndrome
  • Congenital heart diseases
  • Hereditary conduction diseases
  • Hypertrophic cardiomyopathy
  • Short QT-syndrome
  • Sudden cardiac death

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