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بهداشت رواني
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نوشته شده توسط مدير سايت
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۱۲ شهريور ۱۳۸۷ |
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سندرم لندوكلفنر (Landau-Kleffner Syndrome) يا آفازي صرعي اكتسابي يك اختلال نادر از سندرمهاي صرعي اطفال بوده و با پسرفت علمكرد زباني در طفلي كه قبلا تكامل زباني متناسب با سن كسب كرده، همراه با ابنورماليتيهاي صرعي شكل در نوار مغزي و تشنج باليني مشخص مي شود.
Landau-Kleffner syndrome (LKS) is a childhood disorder. A major feature of LKS is the gradual or sudden loss of the
ability to understand and use spoken language. All children with LKS have abnormal electrical brain waves that can be documented by an electroencephalogram (EEG), a recording of the electric activity of the brain. Approximately 80 percent of the children with LKS have one or more epileptic seizures that usually occur at night. Behavioral disorders such as hyperactivity, aggressiveness and depression can also accompany this disorder. LKS may also be called infantile acquired aphasia, acquired epileptic aphasia or aphasia with convulsive disorder. This syndrome was first described in 1957 by Dr. William M. Landau and Dr. Frank R. Kleffner, who identified six children with the disorder.
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