Abstract
Sturge-Weber syndrome is characterized by various symptoms, including facial port-wine nevi, epilepsy, mental retardation, hemiparesis, and glaucoma.A 8 -year-old-girl was referred to our clinic for gingival proliferation at the right side of maxilla. She also had a facial port-wine nevus, epilepsy, and mental retardation. Gingival proliferation was treated by gingivectomy, and the facial port-wine nevus was covered with makeup. This case is described.
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