Jervell and Lange‐Nielsen Syndrome ( <scp>JLNS</scp> ) in a 13‐Year‐Old Girl: A Rare Case Report
JLNS is a rare genetic disorder characterized by congenital sensorineural hearing loss and a prolonged QTc interval, leading to life-threatening arrhythmias. Early diagnosis, beta-blocker therapy, lifestyle modifications, and consideration of ICD surgery are critical in managing sudden cardiac death risk.
Authors
- Muhammad Husnain Ahmad (ORCID: https://orcid.org/0009-0006-5248-0749)
- Humza Saeed (ORCID: https://orcid.org/0009-0003-0256-4272)
- MUHAMMAD REHAN
- Ilsa Babar (ORCID: https://orcid.org/0009-0004-5299-0461)
- Hafiza Iman
- Masab Ali (ORCID: https://orcid.org/0009-0007-8599-6861)
- Sana Javeriya (ORCID: https://orcid.org/0009-0002-5752-4748)
Institutions
- King Edward Medical University (PK)
- Rawalpindi Medical University (PK)
- Punjab Medical College (PK)
Publication Details
- Journal
- Clinical Case Reports
- Published
- 2025-04-01
- DOI
- https://doi.org/10.1002/ccr3.70426
- Primary Topic
- Cardiac electrophysiology and arrhythmias
- Type
- article
- Field-Weighted Citation Impact
- 0.00