Anesthetic Care of a Child Harboring the
Arrhythmia
KCNH2 gene
Long QT syndrome
QT interval
Seizures
Journal
Journal of medical cases
ISSN: 1923-4163
Titre abrégé: J Med Cases
Pays: Canada
ID NLM: 101551824
Informations de publication
Date de publication:
Jan 2022
Jan 2022
Historique:
received:
30
11
2021
accepted:
12
01
2022
entrez:
25
2
2022
pubmed:
26
2
2022
medline:
26
2
2022
Statut:
ppublish
Résumé
Epilepsy is a heterogeneous group of disorders characterized by recurrent and generally unprovoked seizures. Genetic mutations may play an important role in the etiology of epilepsy. Over the past few years, genetic mutations in various genes have been identified in patients with epilepsy. One of the more common mutations responsible for seizures involves the
Identifiants
pubmed: 35211235
doi: 10.14740/jmc3870
pmc: PMC8827253
doi:
Types de publication
Case Reports
Langues
eng
Pagination
40-43Informations de copyright
Copyright 2022, Ghimire et al.
Déclaration de conflit d'intérêts
None to declare.
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