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Case Report
A Case of Klippel-Trenaunay Syndrome Combinded with Sturge-Weber Syndrome
Mi Young Kim, So Young Lee, Na Yeon Kim, Sun Ju Lee, Won Duck Kim, Sung Min Cho, Dong Seok Lee, Doo Kwun Kim, Sung Min Choi
Clin Exp Pediatr. 2003;46(9):909-912.   Published online September 15, 2003
Klippel-Trenaunay syndrome is a rare mesodermal phakomatosis characterized by cutaneous haemangiomata(usually unilateral and involving an extremity), venous varicosities and osseous and soft tissue hypertrophy, of the affected limb. Sturge-Weber syndrome, also a mesodermal pharkomatosis, is characterized by a port-wine nevus, which is present from birth and covers the face and cranium in the territory of the first division of the...
Original Article
Clinical Study on 19 Cases of Neurocutaneous Syndrome in Children.
S H Lee, S J Kim, H D Cha, H S Kim, T C Kwon, C M Kang
Clin Exp Pediatr. 1988;31(3):355-361.   Published online March 31, 1988
The clinical study on 19 cases of neurocutaneous syndrome which were diagnosed at Pediatric Department of Dong San hospital, Keimyung University for last 10 years from Mar. 1975 to Feb. 1985 were performed and following results were obtained. Out of 19 cases, 11 cases were neurofibromatosis, 4 were Tuberous sclerosis and 4 were Sturge- Weber syndrome. 9 cases were male and 10 cases were...
Case Report
A Case of Sturge-Weber Syndrome.
Jun Taek Park, Geom Hyun Jang, Jae Kyu Lee, Kyu Eun Lee, Jung Hyup Oh
Clin Exp Pediatr. 1983;26(8):823-828.   Published online August 31, 1983
We experienced a case of Sturge-Weber Syndrome in 6 month old male. The diagnosis was established by charecteristic features of Sturge-Weber Syndrome such as facial port-wine nevus, focal seizure, hemiparesis, glaucoma and typical calcification & brain atrophy as on brain CT. Plain radiographys of the skull revealed no evidence of calcification, But the brain C.T. clearly showed calcific densities. We have presented this case...