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jervell-lange nielsen syndrome: a case report
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نویسنده
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asgari sogol ,hosseininasab sam mehdi ,behnaz faranak
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منبع
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archives of anesthesiology and critical care - 2025 - دوره : 11 - شماره : 4 - صفحه:606 -609
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چکیده
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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.
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کلیدواژه
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cochlear implantation ,sensorineural hearing loss ,jervell and lange-nielsen syndrome ,long qt syndrome
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آدرس
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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
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پست الکترونیکی
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faranak.behnaz@gmail.com
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Authors
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