Syndrome de nævomatose baso-cellulaire : à propos de deux cas

Nevoid basal cell carcinoma syndrome (NBC) or Gorlin-Goltz syndrome is a hereditary disease with autosomal dominant transmission, complete penetration and variable expressivity. It is characterized by the development abnormalities and a predisposition to various cancers. We present two cases of NBC in young patients documented by standard radiography and computed tomography, highlighting the role of the imaging in this disease.