Aborted Cardiac Arrest in LQT2 Related to Novel
KCNH2
long QT syndrome type 2
mutation
sudden cardiac death
Journal
Medicina (Kaunas, Lithuania)
ISSN: 1648-9144
Titre abrégé: Medicina (Kaunas)
Pays: Switzerland
ID NLM: 9425208
Informations de publication
Date de publication:
16 Jul 2021
16 Jul 2021
Historique:
received:
04
06
2021
revised:
09
07
2021
accepted:
13
07
2021
entrez:
6
8
2021
pubmed:
7
8
2021
medline:
11
8
2021
Statut:
epublish
Résumé
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-go related gene (
Identifiants
pubmed: 34357002
pii: medicina57070721
doi: 10.3390/medicina57070721
pmc: PMC8305506
pii:
doi:
Substances chimiques
ERG1 Potassium Channel
0
Ether-A-Go-Go Potassium Channels
0
KCNH2 protein, human
0
Types de publication
Case Reports
Langues
eng
Sous-ensembles de citation
IM
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