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Gorlin-Goltz syndrome

Author(s): Jawa Deepti | Sircar Keya | Somani Rani | Grover Neeraj | Jaidka Shipra | Singh Sanjeet

Journal: Journal of Oral and Maxillofacial Pathology
ISSN 0973-029X

Volume: 13;
Issue: 2;
Start page: 89;
Date: 2009;
Original page

Keywords: Diagnosis | Gorlin-Goltz syndrome | odontogenic keratocyst

Gorlin-Goltz syndrome is an autosomal dominant inherited disorder characterized by the presence of multiple odontogenic keratocysts along with various cutaneous, dental, osseous, ophthalmic, neurological, and sex organ abnormalities. Early diagnosis is essential as it may progress to aggressive basal cell carcinomas and neoplasias. Gorlin-Goltz syndrome has rarely been reported from India. We report here one such patient, diagnosed at a rural hospital.
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