A novel PTCH1 gene mutation in a pediatric patient associated multiple keratocystic odontogenic tumors of the jaws and Gorlin-Goltz syndrome

• Main Authors: Gozde Ozcan (Author), Burhan Balta (Author), Ahmet Ercan Sekerci (Author), Osman A Etoz (Author), Claudia Martinuzzi (Author), Ozlem Kara (Author), Lorenza Pastorino (Author), Fatma Kocoglu (Author), Omer Ulker (Author), Murat Erdogan (Author)
• Format: Book
• Published: Wolters Kluwer Medknow Publications, 2016-01-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Gorlin-Goltz syndrome (GGS) is an uncommon autosomal dominant inherited disorder which comprises the triad of basal cell carcinomas (BCCs), odontogenic keratocysts, and musculoskeletal malformations. Besides this triad, neurological, ophthalmic, endocrine, and genital manifestations are known to be...