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   jervell-lange nielsen syndrome: a case report  
   
نویسنده asgari sogol ,hosseininasab sam mehdi ,behnaz faranak
منبع archives of anesthesiology and critical care - 2025 - دوره : 11 - شماره : 4 - صفحه:606 -609
چکیده    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.
کلیدواژه cochlear implantation ,sensorineural hearing loss ,jervell and lange-nielsen syndrome ,long qt syndrome
آدرس shahid beheshti university of medical sciences, anesthesiology research center, iran, shahid beheshti university of medical sciences, anesthesiology research center, iran, shahid beheshti university of medical sciences, school of medicine, shohada-e-tajrish hospital, department of anesthesiology, iran
پست الکترونیکی faranak.behnaz@gmail.com
 
     
   
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