Genetics, Clinical Features, and Long-Term Outcome of Noncompaction Cardiomyopathy

The clinical outcomes of noncompaction cardiomyopathy (NCCM) range from asymptomatic to heart failure, arrhythmias, and sudden cardiac death. Genetics play an important role in NCCM. This study investigated the correlations among genetics, clinical features, and outcomes in adults and children diagn...

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Veröffentlicht in:	Journal of the American College of Cardiology 2018-02, Vol.71 (7), p.711-722
Hauptverfasser:	van Waning, Jaap I., Caliskan, Kadir, Hoedemaekers, Yvonne M., van Spaendonck-Zwarts, Karin Y., Baas, Annette F., Boekholdt, S. Matthijs, van Melle, Joost P., Teske, Arco J., Asselbergs, Folkert W., Backx, Ad P.C.M., du Marchie Sarvaas, Gideon J., Dalinghaus, Michiel, Breur, Johannes M.P.J., Linschoten, Marijke P.M., Verlooij, Laura A., Kardys, Isabella, Dooijes, Dennis, Lekanne Deprez, Ronald H., IJpma, Arne S., van den Berg, Maarten P., Hofstra, Robert M.W., van Slegtenhorst, Marjon A., Jongbloed, Jan D.H., Majoor-Krakauer, Danielle
Format:	Artikel
Sprache:	eng
Schlagworte:	Adults Cardiac arrhythmia Cardiology Cardiomyopathy Children Correlation analysis Deoxyribonucleic acid DNA Electrocardiography Family medical history Genes Genetic counseling Genetic testing Genetics Heart Heart diseases Heart failure LVNC Medical prognosis Medical records Mutation NMR noncompaction cardiomyopathy Nuclear magnetic resonance outcome Patients prognosis Risk Studies Ventricle
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