Journal of Pediatric Neurology 2013; 11(01): 051-054
DOI: 10.3233/JPN-120587
Georg Thieme Verlag KG Stuttgart – New York

Sturge-Weber syndrome without facial nevus

Ibrahim Guler
a   Department of Radiology, Meram Medical Faculty, Necmettin Erbakan University, Konya, Turkey
,
Ahmet Kucukapan
a   Department of Radiology, Meram Medical Faculty, Necmettin Erbakan University, Konya, Turkey
,
Demet Kiresi
a   Department of Radiology, Meram Medical Faculty, Necmettin Erbakan University, Konya, Turkey
› Author Affiliations

Subject Editor:
Further Information

Publication History

07 March 2012

19 June 2012

Publication Date:
30 July 2015 (online)

Abstract

Sturge-Weber syndrome is a rare neurocutaneous disorder. Coexistence of facial nevus with epilepsy often suggests the diagnosis of Sturge-Weber syndrome. However, the diagnosis becomes more difficult when there is no facial nevus. Radiologic examinations are often used for diagnosis and management. Especially in cases without skin findings, the radiological examinations with typical findings become more important. In this paper, we report case of a 12-year-old girl who was followed with the diagnosis of epilepsy since the age of two years, had complaints of weakness of the left arm and left leg without skin findings, and was diagnosed with Sturge-Weber syndrome after radiological examinations.