Oral and extraoral manifestationse of sturge-Weber syndrome: A rare finding

Abstract

Sturge-Weber syndrome (SWS) is a rare congenital developmental disorder characterized by unilateral cutaneous vascular malformation (nevus flammeus or port-wine stains) in association with ipsilateral leptomeningeal angiomatosis and glaucoma. This article presents a case of SWS associated with gingival hyperplasia and pyogenic granuloma.

Keywords

• Congenital developmental disorder
• neurocutaneous ocular disorder
• pyogenic granuloma