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Simultaneous Catecholaminergic Polymorphic Ventricular Tachycardia and Long QT Syndrome Gene Mutations.
Lakhana, Muhddesa; McGee, James; George, Blessen; Whang, William; Kanner, Lawrence; Park, Won Jun.
Afiliação
  • Lakhana M; Internal Medicine, Mount Sinai South Nassau, Oceanside, USA.
  • McGee J; Internal Medicine, Mount Sinai South Nassau, Oceanside, USA.
  • George B; Internal Medicine, Mount Sinai South Nassau, Oceanside, USA.
  • Whang W; Cardiology, Icahn School of Medicine at Mount Sinai, New York, USA.
  • Kanner L; Cardiology, Mount Sinai South Nassau, Oceanside, USA.
  • Park WJ; Cardiology, Mount Sinai South Nassau, Oceanside, USA.
Cureus ; 13(11): e19195, 2021 Nov.
Article em En | MEDLINE | ID: mdl-34873534
ABSTRACT
Genetic channelopathies can predispose individuals to life-threatening arrhythmias. Two such channelopathies are long QT syndrome (LQTS) and catecholaminergic polymorphic ventricular tachycardia (CPVT). To the best of our knowledge, we present the first case of LQTS with novel combined genetic mutations of KCNH2 and cardiac ryanodine receptor (RYR2) genes.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Cureus Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Cureus Ano de publicação: 2021 Tipo de documento: Article