Gorlin-Goltz syndrome: A rare case report

Gorlin-Goltz syndrome: A rare case report

Gorlin-Goltz syndrome is an uncommon autosomal dominant inherited disorder characterized by numerous basal cell carcinomas, odontogenic keratocysts (OKCs) and musculoskeletal malformations. A rare case of this syndrome observed in a 13-year-old male patient is presented in which multiple OKCs were c...

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Bibliographic Details
Main Authors: Chetan A Pol, Suvarna K Ghige, Ritesh R Kalaskar, Suchitra R Gosavi
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2013-01-01
Series:Contemporary Clinical Dentistry
Subjects:
Calcification of falx cerebri
Gorlin-Goltz syndrome
nevoid basal cell carcinoma syndrome
odentogenic keratocyst
Palmar pits
Online Access:http://www.contempclindent.org/article.asp?issn=0976-237X;year=2013;volume=4;issue=4;spage=547;epage=550;aulast=Pol

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http://www.contempclindent.org/article.asp?issn=0976-237X;year=2013;volume=4;issue=4;spage=547;epage=550;aulast=Pol

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