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An Official Publication of the Indian Association of Oral and Maxillofacial Pathologists


 
CASE REPORT Table of Contents   
Year : 2009  |  Volume : 13  |  Issue : 2  |  Page : 89-92
Gorlin-Goltz syndrome


1 Department of Pedodontics and Preventive Dentistry, D.J. College of Dental Sciences and Research, Niwari Road, Modinagar, Uttar Pradesh, India
2 Department of Oral and Maxillofacial Pathology, D.J. College of Dental Sciences and Research, Niwari Road, Modinagar, Uttar Pradesh, India

Correspondence Address:
Keya Sircar
Department of Oral and Maxillofacial Pathology, D.J. College of Dental Sciences and Research, Niwari Road, Modinagar, Uttar Pradesh
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0973-029X.57677

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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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