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Year : 2013  |  Volume : 2  |  Issue : 2  |  Page : 150-153

Gorlin-Goltz syndrome: A rare case report

1 Department of Oral Pathology, Government Dental College, Vijayawada, Andhra Pradesh, India
2 Department of Oral Pathology, Dr. Sudha and Nageshwara Rao Siddartha Institute of Dental Sciences, Vijayawada, Andhra Pradesh, India
3 Department of Periodontics, Institute of Dental Sciences, Bareilly, Uttar Pradesh, India
4 Department of Orthodontics, Institute of Dental Sciences, Bareilly, Uttar Pradesh, India

Correspondence Address:
Srikanth Guduguntla
Department of Periodontics, Institute of Dental Sciences, Bareilly, Uttar Pradesh
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/2277-8632.112358

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Gorlin-Goltz syndrome is an inherited autosomal dominant disorder characterized by the presence of multiple odontogenic keratocysts of jaws, basal cell carcinomas, palmar, plantar pits and intracranial calcifications. Apart from these many dental, skeletal, ophthalmic and neurological abnormalities have been reported. Here, we present a case of familial Gorlin-Goltz Syndrome, characterized by multiple odontogenic cysts, calcification of falx cerebri, hypertelorism and neurologic disorder.

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