Revista Habanera de Ciencias Médicas
versão On-line ISSN 1729-519X
The so called Gorlin’s Syndrome is a rare infrequent clinical pathological disorder with a well known and multi expression hereditary autosomic dominant characteristic pattern. The syndrome is characterized by multiple nodules in non exposed skin and facial skin which tend to become malignant with age (basal cell moles), multiple odontogenic keratocysts, and hypertelorism, a wide nose base among others. Our main purpose is to update the subject as well as to present the case diagnosed as a Gorlin’s Syndrome in the plastic surgery department of CalixtoGarciaHospital.
Palavras-chave : Gorlins Syndrome; Multiple keratocysts.