Gorlin-Goltz syndrome: A rare case report

Gorlin-Goltz syndrome (GGS) is an autosomal dominant disorder with a high degree of penetrance and variable expressivity. It is a rare phakomatosis characterized by multiple odontogenic keratocysts (OKCs), bifid ribs, and other abnormalities. The incidence of the GGS is estimated at 1 in 57,000–1 in...

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Bibliographic Details
Main Authors: Naveen N Kumar, S Padmashree, T R Jyotsna, Shilpa Padar Shastry
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2018-01-01
Series:Contemporary Clinical Dentistry
Subjects:
Online Access:http://www.contempclindent.org/article.asp?issn=0976-237X;year=2018;volume=9;issue=3;spage=478;epage=483;aulast=Kumar