Jervell and Lange‐Nielsen Syndrome (JLNS) in a 13‐Year‐Old Girl: A Rare Case Report

ABSTRACT 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 card...

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Principais autores:	Masab Ali, Sana Javeriya, Muhammad Husnain Ahmad, Ilsa Babar, Muhammad Maaz Bin Rehan, Hafiza Iman, Humza Saeed
格式:	Artigo
語言:	Inglês
出版:	Wiley 2025-04-01
叢編:	Clinical Case Reports
主題:	genetic counseling genetic testing implantable defibrillators Jervell and Lange‐Nielsen syndrome sensorineural hearing loss torsades de pointes
在線閱讀:	https://doi.org/10.1002/ccr3.70426
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