Aborted Cardiac Arrest in LQT2 Related to Novel KCNH2 (hERG) Variant Identified in One Lithuanian Family

Congenital long QT syndrome (LQTS) is a hereditary ion channelopathy associated with ventricular arrhythmia and sudden cardiac death starting from young age due to prolonged cardiac repolarization, which is represented by QT interval changes in electrocardiogram (ECG). Mutations in human ether-à-go-...

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Detalles Bibliográficos
Autores principales: Bileišienė, Neringa, Barysienė, Jūratė, Mikštienė, Violeta, Preikšaitienė, Eglė, Marinskis, Germanas, Keževičiūtė, Monika, Utkus, Algirdas, Aidietis, Audrius
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8305506/
https://www.ncbi.nlm.nih.gov/pubmed/34357002
http://dx.doi.org/10.3390/medicina57070721

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8305506/
https://www.ncbi.nlm.nih.gov/pubmed/34357002
http://dx.doi.org/10.3390/medicina57070721

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