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

Year: 2025
Type: article
Study design: 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 cardiac death risk.
Language: English
Field: Medicine
Open Access status: gold
Estimated APC paid: $1,820
OpenAlex ID: W4409558033
FWCI:
Cites: 11
Cited by:
Related to: 10