Molecular Identification and Successful Treatment with Targeted Therapy in Gorlin Syndrome: A Case Report
Case Report Open Access
Gorlin Syndrome (GS), is a rare autosomal dominant cancer predisposition disorder, frequently under-diagnosed. It is characterized by the presence of multiple Basal Cell Carcinomas (BCCs), odontogenic keratocysts, palmoplantar pits, and many other developmental anomalies and neoplasms.