Overlap of Congenital Deafness and Long QT Syndrome With Distinct Genetic Basis

Long QT syndrome in combination with deafness should be confirmed with genetic testing, as their combined presence can be a coincidental finding.

Authors

Institutions

Publication Details

Journal
JACC Case Reports
Published
2026-01-21
DOI
https://doi.org/10.1016/j.jaccas.2025.106521
Primary Topic
Cardiac electrophysiology and arrhythmias
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Overlap of Congenital Deafness and Long QT Syndrome With Distinct Genetic Basis

M Badrul Alam, Faisal Qadir, Romana Pirah, Arshad Ali et al.
JACC Case Reports
Cardiac electrophysiology and arrhythmias
article

Overlap of Congenital Deafness and Long QT Syndrome With Distinct Genetic Basis

M Badrul Alam, Faisal Qadir, Romana Pirah, Arshad Ali, Zubair Mumtaz, Muhammad Mohsin
article en

Abstract

Long QT syndrome in combination with deafness should be confirmed with genetic testing, as their combined presence can be a coincidental finding.

JACC Case ReportsVol. 31(9)
National Institute of Cardiovascular Diseases (PK)
Openalex Percentile: Top 84%
Cardiac electrophysiology and arrhythmias
DOIOpen Access PDFOpenAlex
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Overlap of Congenital Deafness and Long QT Syndrome With Distinct Genetic Basis — M Badrul Alam, Faisal Qadir, et al. · JACC Case Reports (2026) | TGRS Research Map | TGRS