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제1형 신경섬유종증의 임상적 고찰
A Clinical Study on Neurofibromatosis type 1제1형 신경섬유종증의 임상적 고찰
김규한 ( Kyu Han Kim ) , 조광현 ( Kwang Hyun Cho ) , 정진호 ( Jin Ho Chung ) , 박경찬 ( Kyoung Chan Park ) , 은희철 ( Hee Chul Eun ) , 윤상웅 ( Sang Woong Youn ) , 박경찬 ( Kyoung Chan Park ) , 김규한 ( Kyu Han Kim ) , 조광현 ( Kwang Hyun Cho ) , 정진호 ( Jin Ho Chung ) , 은희철 ( Hee Chul Eun ) , 윤재일 ( Jai Il Youn ) , 유희준 , 손숙자 , 김태흥 , 김도원 , 전재복
UCI I410-ECN-0102-2009-510-005438487

Background : Neurofibiomat,osis type 1(NF-1) is a multisystemic disorder of genetic ori gin, affecting one in every 3000 to 4000 people. It is clinically important in the aspect of dermatology, pediatrics, orthopedic surgery, neurology, neurosurgery and ophthalmology. Objective : The purpore of this study was to elucidate the clinical characteristics of NF-1 in Korean people. Methods : We carried out a retrospective study on 112 patients which were compatible to the diagnostic criteria of Riccardi and Neurofibromatosis Conference Statement. The results were compared with other western studies. Results : The age of onset, sex ratio, family history of neurofibromatosis, and clinica features of cafe-au-lait spot, neurofibroma, and axillary freckinings did not differed from western countries. However, some characterist,ics of NF 1(e.g. Lisch nodule) were not as sessed in the most of the cases and incomplete evaluations of the systemic diseases wen found. Conclusion : In this study t.he clinial features of NF-1 did not differ from western coun tries in many aspects. A more intensive evaluation of patient,s status is needed to manag; NF-1 patients appropritely. (Kor J Dermatol 1995;33(6): 1091-1098)

[자료제공 : 네이버학술정보]
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