
Overt long QT syndrome in children presenting with seizure disorders in Pakistan
Author(s) -
Usman Rashid,
Ahmad Omair Virk,
Rashid Nawaz,
Tahir Mahmood,
Zile Fatima
Publication year - 2021
Publication title -
annals of pediatric cardiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.292
H-Index - 19
eISSN - 0974-2069
pISSN - 0974-5149
DOI - 10.4103/apc.apc_10_21
Subject(s) - medicine , seizure disorders , pediatrics , epilepsy , long qt syndrome , psychiatry , qt interval
The long QT syndrome (LQTS) is a repolarization defect of heart involving potassium linked channels and it usually manifests clinically as seizures, syncope, or sudden cardiac death syndrome in children secondary to its characteristic ventricular tachy-arrhythmia like torsades de pointes. The reason behind epilepsy or seizures like activity in this disease is the sequelae of prolonged cerebral hypoperfusion secondary to the cardiac dysrhythmia. The aim of study is to look for clinical spectrum and risk factors associated with LQTS among children presenting with epilepsy, which can predict the early diagnosis of LQTS.