Cargando…
Congenital Short QT Syndrome
The Short QT Syndrome is a recently described new genetic disorder, characterized by abnormally short QT interval, paroxysmal atrial fibrillation and life threatening ventricular arrhythmias. This autosomal dominant syndrome can afflict infants, children, or young adults; often a remarkable family b...
Autores principales: | Crotti, Lia, Taravelli, Erika, Girardengo, Giulia, Schwartz, Peter J |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Indian Heart Rhythm Society
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2811207/ https://www.ncbi.nlm.nih.gov/pubmed/20126594 |
Ejemplares similares
-
Congenital long QT syndrome
por: Crotti, Lia, et al.
Publicado: (2008) -
Multiscale Complexity Analysis of the Cardiac Control Identifies Asymptomatic and Symptomatic Patients in Long QT Syndrome Type 1
por: Bari, Vlasta, et al.
Publicado: (2014) -
Congenital Short QT Syndrome
por: Antzelevitch, Charles, et al.
Publicado: (2004) -
From gene-specific to function-specific risk stratification in long QT syndrome Type 2: implications for clinical management
por: Crotti, Lia
Publicado: (2023) -
QT Adaptation and Intrinsic QT Variability in Congenital Long QT Syndrome
por: Seethala, Srikanth, et al.
Publicado: (2015)