http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
남기순 ( Ki Soon Nam ),이혜진 ( Hye Jin Lee ),황규왕 ( Kyu Uang Whang ),김영근 ( Young Keun Kim ) 대한피부과학회 1996 대한피부과학회지 Vol.34 No.1
Piebaldism is a rare autosomal dominant genetic disorder characterized by localized and stationary hypomelanosis of skin and hair secondary to an absence of melanocytes in the involved skin. Depigmentation in piebalrlism shows a characteristic distribution that involves the forehead, ventral chest, abdomen, and extremities. Cases of piebaldism have been reported in association with extracutaneous abnormalities such as heterochromia irides, osteopathia striata, deafness, mental retardation, and Hirschsprung's disease. We report a case of piebaldism associated with strabismus and torticollis in a 6-year-old female patient. Piebaldism associated with strabismus and torticollis has not been reported in any previous literature. (Kor J Dermatol 1996;34(1): 151-154)
Statistical Errors in Papers in the two Korean Dermatology Journals
이종숙,이성열,남기순 대한피부과학회 1996 Annals of Dermatology Vol.8 No.1
Background: Statistical errors have been noted in a large percentage of articles appearing in medical journals. Their incidence in the Annals of Dermatology and the Korean Journal of Dermatology, however, has not been studied. Objective: The purpose of this study was to evaluate the accuracy of statistical methods in the Annals of Dermatology and the Korean Journal of Dermatology Method: Original papers using the t test in the Annals of Dermatology(AD) and in the Korean Journal of Dermatology(KJD) from January 1990 to July 1994 were analyzed for correctness of statistical methods. Results: Of the 376 original papers in the period considered, 78(20.7%) presented t tests and 43(55.1%) of these also contained some errors. Of the 9 papers from the Annals of Dermatology, 4(44.4%) included at least one error. Of the 69 papers from the Korean Journal of Dermatology, 39(56.5%) included at least one error. Conclusion: Misuse of statistical methodology may not be uncommon in the two Korean Dermatology Journals, and it would be prudent to give more attention to statistical methodology
A Case of Hunter ` s Syndrome With Ivory - colored Papules
KIM, Young Keun,남기순,Whang, Kyu Uang,이정율 대한피부과학회 1996 Annals of Dermatology Vol.8 No.1
We report a case of Hunter's syndrome with characteristic nodules on the upper back. The patient was a 7-year-old Korean boy who presented with ivory-colored papules and nodules on both sides of the scapula, pectoral regions and lateral aspects of the upper arms. These lesions are regarded as pathognomonic cutaneous markers for Hunter s syndrome. He also presented with truncal hypertrichosis, retarded growth, short neck, round face, claw like contractures of hands, multiple joint contractures, and a clear cornea. Severely elevated glycosaminoglycan levels were present in the patient's urine samples. The patient's 5-year-old brother had similar clinical features.