Gorlin-Goltz syndrome: A rare case report

Abstract

Gorlin-Goltz syndrome is an inherited autosomal dominant disorder characterized by the presence of multiple odontogenic keratocysts of jaws, basal cell carcinomas, palmar, plantar pits and intracranial calcifications. Apart from these many dental, skeletal, ophthalmic and neurological abnormalities have been reported. Here, we present a case of familial Gorlin-Goltz Syndrome, characterized by multiple odontogenic cysts, calcification of falx cerebri, hypertelorism and neurologic disorder.