Gorlin Goltz syndrome: A case report

Gorlin-goltz syndrome is an autosomal dominant disorder principally characterized by cutaneous basal cell carcinomas, multiple keratocystic odontogenic tumors(kcots), and skeletal anomalies. in addition to the classical triad described by gorlin and goltz, other neurological, ophthalmic, endocrine, and genital manifestations have also been established as features of the syndrome. in this report a 12-year-old male patient with gorlin-goltz syndrome and its teratment is presented with 1.5 year follow up period. the aim of this case report is to increase the awareness of the syndrome among dentists about younger age patients with no lesions of the skin and emphesize the importance of early diagnosis.