Agrupación familiar de prolapso de la válvula mitral en la comunidad

Francesca N Delling1, Jian Rong2, Martin G Larson2

  • 1From Boston University and National Heart, Lung, and Blood Institute's Framingham Heart Study, Framingham, MA (F.N.D., J.R., M.G.L., B.L., E.O., P.S., E.J.B., R.S.V.); Department of Medicine (Cardiovascular Division), Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA (F.N.D.); Section of Neurology (J.R.), Section of Cardiology (E.J.B., R.S.V.), and Preventive Medicine (E.J.B., R.S.V.) sections in the Department of Medicine, Boston University School of Medicine, Boston, MA; Section of Mathematics and Statistics, Boston University, Boston, MA (M.G.L.); and Center for Human Genetic Research (S.A.S.) and Cardiac Ultrasound Laboratory, Department of Medicine (R.A.L.), Massachusetts General Hospital, Harvard Medical School, Boston. fdelling@bidmc.harvard.edu.

Circulation
|November 2, 2014
PubMed
Resumen

El prolapso de la válvula mitral parental (MVP) y las morfologías de MVP no diagnosticadas aumentan el riesgo de MVP en la descendencia. Este estudio pone de relieve la base genética de MVP y la importancia de estas condiciones menos definidas.

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