INFORMAZIONI SU QUESTO ARTICOLO
Pubblicato online: 09 ott 2009
Pagine: 61 - 64
DOI: https://doi.org/10.2478/v10034-009-0002-z
Parole chiave
This content is open access.
Gorlin's syndrome (GS) is a rare autosomal, dominant syndrome, characterized by multiple basal cell carcinomas, odontogenic keratocysts, a characteristic facial appearance, skeletal anomalies and malignancies of various organs throughout the body. We describe a 14-year-old girl with GS and propose a management protocol.