GOLTZ GORLIN SYNDROME- A CASE REPORT WITH OVERVIEW

Abstract

Goltz Gorlin syndrome (GGS) is an multisystemic disease with an autosomal dominant disorder, with complete variance, though irregular cases have been described. This article includes a case report and an extensive review of the GGS with regard to its history, incidence, etiology, features, investigations, diagnostic criteria, keratocystic odontogenic tumor and treatment modalities. case of a 32-year-old female patient presenting with three major features of Gorlin-Goltz syndrome. Radiologic findings of the syndrome are easily identifiable on Orthopantomogram, cbct scans. These investigations prompt an early verification of the disease, which is very important to prevent recurrence and better survival rates from the coexistent diseases.