A Case Report of the Sturge-Weber Syndrome |
Ki Yong Park1, Chung Kyu Kim1, Sung Hoon Cho1, Chang Nak Choi2 |
1Department of Pediatrics, Catholic Medical College Seoul, Korea 2Department of Neuro-Surgery Catholic Medical College Seoul, Korea |
Sturge-Weber Syndrome 의 1 예 |
박기용1, 김정규1, 조성훈1, 촤창락2 |
1가톨릭의과대학 소아과학교실 2가톨릭의과대학 신경외과학교실 |
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Abstract |
This is a case report of the Sturge-Weber Syndrome. The case was a 10-year-old girl who entered at Dept, of Pediatrics, St. Mary’s hospital in July 1969 with complaints of headache, vomiting and pain in the both lower extremities. The diagnosis was established by characteristics features of Sturge-Weber Syndrome such as portwine nevus, convulsive disorder, some degree of metal retardation and typical intracranial calcification in left paietooccipital area.
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