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novel association between scn1a mutation and central sleep apnea: a case of basilar-type migraine
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نویسنده
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esmaeili nazanin ,hasani arian ,saleh nejad tayebeh ,amirifard hamed
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منبع
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case reports in clinical practice - 2025 - دوره : 10 - شماره : 1 - صفحه:23 -28
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چکیده
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We report a 37-year-old woman with recurrent episodes of excessive daytime sleepiness, bizarre behavior, social delays, and confusion lasting 3–5 days. between episodes, she experienced only mild migraine-like headaches. genetic testing identified an scn1a mutation, which may cause central sleep apnea, basilar-type migraine, and a channelopathy-related encephalopathic state in her. this is the first report linking an scn1a mutation with central sleep apnea. we recommend future cohort studies to clearly examine the association between scn1a mutation and central sleep apnea.
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کلیدواژه
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scn1a mutation ,central sleep apnea ,basilar-type migraine ,sleep disorders ,genetic mutation ,migraine pathophysiology
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آدرس
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tehran university of medical sciences, autonomous nervous system (ans) association, students’ scientific research center (ssrc), iran, tehran university of medical sciences, autonomous nervous system (ans) association, students’ scientific research center (ssrc), iran, ronash medical genetics laboratory, department of molecular genetics, iran, tehran university of medical sciences, imam khomeini hospital complex, department of neurology, iran
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پست الکترونیکی
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dr.amirifard@gmail.com
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Authors
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