This document discusses Gorlin Goltz Syndrome, a rare genetic condition caused by mutations in the PTCH1 gene. It presents three key points: 1. Gorlin Goltz Syndrome is characterized by multiple basal cell carcinomas, odontogenic keratocysts of the jaws, and other abnormalities like skeletal anomalies and ovarian fibromas. It has an autosomal dominant inheritance pattern. 2. The case presentation describes a 32-year-old female patient found to have multiple recurrent odontogenic keratocysts in the mandible and maxilla, leading to a diagnosis of Gorlin Goltz Syndrome based on major and minor diagnostic criteria. 3. Management of odontogenic kerat