TY - JOUR A1 - Krishnamurthy, Vasavi A1 - Bhatnagar, Sunanda A1 - Pagare, S T1 - Gorlin-Goltz Syndrome Y1 - 2015/1/1 JF - Indian Journal of Oral Health and Research JO - Indian J Oral Health Res SP - 29 EP - 32 VL - 1 IS - 1 UR - https://www.ijohr.org/article.asp?issn=2393-8692;year=2015;volume=1;issue=1;spage=29;epage=32;aulast=Krishnamurthy DO - 10.4103/2393-8692.158908 N2 - Gorlin-Goltz syndrome is an autosomal dominant disorder showing multiple organ involvement. The syndrome consists principally of nevoid basal cell carcinomas, keratocystic odontogenic tumors (KCOT), skeletal anomalies and intracranial calcifications. A case report of a 25-year-old female patient emphasizing its clinical and radiographic manifestations is presented in this article. Radiographs and computed tomography showed recurrent, multilocular and expansile lesions, which were examined histologically, confirming the diagnosis of KCOT. Skin lesions in the form of palmar pits and solitary pigmented nevi were seen. The sella turcica was bridged and the right fifth rib was bifid. The bilamellar falx cerebri calcification was confirmed on computed tomography of brain. The patient was treated and explained about the prognosis. ER -