Jervell-Lange Nielsen Syndrome: A Case Report
There is a rare genetic disorder called Jervell-Lange Nielsen syndrome that leaves people congenitally deaf and with a long QT interval. This can lead to deadly heart rhythm problems and sudden death. For the treatment of hearing loss, cochlear implants, and for the treatment of heart difficulties, beta-blockers, and in certain circumstances, implantable cardioverter defibrillators, arrhythmias, syncope attacks, and sudden death are recommended. We discuss the case of an 8-year-old child who was referred for cochlear implantation after being diagnosed with Jervell-Lange Nielsen syndrome. In this study, we want to deal with patient management preoperatively and during surgery and describe the side effect of this syndrome
Authors
- Faranak Behnaz (ORCID: https://orcid.org/0000-0003-2856-3975)
- Sogol Asgari (ORCID: https://orcid.org/0000-0001-7837-8888)
- Seyed Sam Mehdi Hosseininasab (ORCID: https://orcid.org/0009-0008-7775-6443)
Institutions
- Shahid Beheshti University of Medical Sciences (IR)
Publication Details
- Journal
- Archives of Anesthesia and Critical Care
- Published
- 2025-08-19
- DOI
- https://doi.org/10.18502/aacc.v11i4.19383
- Primary Topic
- Fetal and Pediatric Neurological Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00