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Article in English | MEDLINE | ID: mdl-18204747

ABSTRACT

Gorlin-Goltz syndrome, also known as basal cell nevus syndrome, is an uncommon, autosomal dominant inherited disorder, which is characterized by numerous basal cell carcinomas, maxillary keratocysts, and musculoskeletal malformations. Occasionally, it is associated with aggressive basal cell carcinomas and internal malignancies. Early diagnosis and treatment are essential, as well as genetic counseling. A patient with characteristic symptoms of nevoid basal cell carcinomas and a review of the literature are presented.


Subject(s)
Basal Cell Nevus Syndrome , Carcinoma, Basal Cell , Facial Neoplasms , Skin Neoplasms , Basal Cell Nevus Syndrome/diagnosis , Basal Cell Nevus Syndrome/genetics , Basal Cell Nevus Syndrome/surgery , Carcinoma, Basal Cell/genetics , Carcinoma, Basal Cell/surgery , Facial Neoplasms/genetics , Facial Neoplasms/surgery , Humans , Male , Middle Aged , Skin Neoplasms/genetics , Skin Neoplasms/surgery
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