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Odontogenic Keratocysts in Gorlin-Goltz Syndrome: A Case Report.

Abstract
Gorlin-Goltz syndrome is an autosomal dominant inherited condition comprising the principle triad of basal cell carcinomas, multiple jaw keratocysts, and skeletal anomalies. The presence of jaw cysts are the early diagnostic feature of this syndrome, and this can be incidentally identified by routine radiographs. A patient presented with signs and symptoms of Gorlin-Goltz syndrome to us in her early stages.
AuthorsSatheesh Chandran, Karthikeyan Marudhamuthu, R Riaz, Saravanan Balasubramaniam
JournalJournal of international oral health : JIOH (J Int Oral Health) Vol. 7 Issue Suppl 1 Pg. 76-9 ( 2015) ISSN: 0976-7428 [Print] India
PMID26225111 (Publication Type: Case Reports)

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