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Sturge - Weber 증후군의 문헌고찰과 증례보고
임재석(Jae Suk Rim),김성문(Sung Moon Kim),유재준(Jae Jun Ryu),김온(Onn Kim) 대한악안면성형재건외과학회 1989 Maxillofacial Plastic Reconstructive Surgery Vol.11 No.2
Sturge-Weber syndrome은 드물게 볼 수 있는 선천성질환으로 일명 encephalotrigeminal angiomatosis, 또는 Sturge-Weber syndrome 이라 하며 삼차신경의 분지를 따라 분포하는 안면 혈관종, 안면 혈관종과 같은 부위의 intracerebral calcification 경련의 특징을 가진다. 이에 저자들은 Sturge-Weber syndrome 3예를 치험하였기에 문헌고찰과 함께 보고하는 바이다. Sturge-Weber Syndrome is a congenital disorder and characterized by facial hemangioma following one or more divisions of the trigeminal nerve, epilepsy, mental retardation, contralateral hemiplegia, occlular involvement, gingival involvement. A 34 year old Korean man, a 25 year old Korean woman and a 48 year old Korean woman were found to have red - purple colored pigmentation on the hemifacial area and upper oral mucosal area
STURGE-WEBER SYNDROME: REPORT OF THREE CASES
Kim,Onn,Rim,Jae Suk,Kim,Sung Moon,Ryu,Jae Jun 大韓顎顔面成形再建外科學會 1989 Maxillofacial Plastic Reconstructive Surgery Vol.11 No.2
Sturge - Weber Syndrome is a congenital disorder and characterized by facial hemangioma following one or more divisions of the trigeminal nerve, epilepsy, mental retardation, contralateral hemiplegia, occlualr involvement, gingival involvement. A 34 year old Korean man, a 25 year old Korean Woman and a 48 year old Korean woman were found to have red - purple colored pigmentation on the hemifacial area and upper oral mucosal area.