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»ó¿°»öü ¿ì¼º ¾ß°£ ÀüµÎ¿± °£Áú·Î ÃßÁ¤µÇ´Â ȯ¾Æ 1¿¹ A Case of Suspected Autosomal Dominant Nocturnal Frontal Lobe Epilepsy

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±è¼±¿µ/Seon Young Kim ¹ÚÃæä/±èÈﵿ/Á¤ÈñÁ¤/Jung Chae Park/Heung Dong Kim/Hee Jung Chung

Abstract

ÀúÀÚµéÀº 3³â µ¿¾È Áö¼ÓÀûÀ¸·Î ¹Ýº¹µÇ´Â ¼ö¸éÀå¾Ö Áõ»óÀ» ÁÖ¼Ò·Î ³»¿øÇÑ 5¼¼ ³²¾Æ¿¡¼­ Áö¼ÓÀû ºñµð¿À-³úÆÄ °Ë»ç·Î È®ÀÎµÈ »ó¿°»öü ¿ì¼º ¾ß°£ ÀüµÎ¿± °£Áú·Î ÃßÁ¤µÇ´Â 1·Ê¸¦ °æÇèÇÏ¿´±â¿¡ º¸°íÇÏ´Â ¹ÙÀÌ´Ù.

Autosomal dominant nocturnal frontal lobe epilepsy(ADNFLE) is a recently identified partial epilepsy. This disorder is characterized by a variable age of onset(mostly in childhood), autosomal dominant inheritance, clusters of brief frontal
nocturnal
seizures, negative findings on neuroimaging, and fairly good prognosis. Carbamazepine is known to be the most useful drug in this type of epilepsy.
We experienced a case of 5-year-old boy who had unusual arousal and irritability every night for 3 yeats and had sharp & wave discharges from frontal lobe region in long-term video-EEG monitoring, who was suspected as an autosomal dominant
nocturnal
frontal lobe epilepsy.
We report a case with a brief review of literatures.

Å°¿öµå

Autosomal dominant nocturnal frontal lobe epilepsy; Long-term video-EEG monitoring;

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