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National Journal of Maxillofacial Surgery
 
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CASE REPORT
Year : 2010  |  Volume : 1  |  Issue : 1  |  Page : 50-52

Gorlin-Goltz syndrome


1 Department of Oral and Maxillofacial Surgery, Saraswati Dental College and Hospital, Lucknow, Uttar Pradesh, India
2 Department of Anesthesiology, King George Medical College , Lucknow, Uttar Pradesh, India

Correspondence Address:
Munish Kohli
Principal and Head, Department of Oral and Maxillofacial Surgery, Saraswati Dental College and Hospital, 233 Tiawri Ganj, Lucknow, Uttar Pradesh
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0975-5950.69171

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Gorlin-Goltz syndrome is an inherited autosomal dominant disorder with complete penetrance and extreme variable expressivity. The authors present a case of an 11-year-old girl with typical features of Gorlin-Goltz syndrome with special respect to medical and dental problems which include multiple bony cage deformities like spina bifida with scoliosis having convexity to the left side, presence of an infantile uterus and multiple odonogenic keratocysts in the maxillofacial region.


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