SturgeWeber syndrome is a rare congenital neurological and skin disorder. The pathognomic features of disease include angioma of the leptomeninges, facial nevus, convulsions and gingival hyperplasia. In the present case, a 30yearold male patient presented with a port wine stain on the right side of the face, dilated blood vessels of the right eye, epilepsy and intraorally with gingival enlargement in both maxillary and mandibular arches.

Keywords: SturgeWeber Syndrome; Port Wine Stain; Gingival Enlargement.