Andersen-Tawil syndrome: a review of its clinical and genetic diagnosis with emphasis on cardiac manifestations

The Andersen-Tawil syndrome is a cardiac ion channel disease that is inherited in an autosomal dominant way and is classified as type 7 of the congenital long QT syndromes. Affected gene is KCNJ2, which forms the inward rectifier potassium channel designated Kir2.1. This protein is involved in stabi...

Ausführliche Beschreibung

Bibliographische Detailangaben

Veröffentlicht in:	Archivos de cardiología de México 2014-10, Vol.84 (4), p.278-285
Hauptverfasser:	Márquez, Manlio F, Totomoch-Serra, Armando, Vargas-Alarcón, Gilberto, Cruz-Robles, David, Pellizzon, Oscar A, Cárdenas, Manuel
Format:	Artikel
Sprache:	spa
Schlagworte:	Andersen Syndrome - complications Andersen Syndrome - diagnosis Andersen Syndrome - genetics Heart Diseases - etiology Humans Pedigree
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!