Gorlin Syndrome

Author(s):
Masoomeh ShirzaiiMasoomeh Shirzaii1, Sirous  Risbaf Fakour Sirous Risbaf Fakour 2,*
1Department of Oral and Maxillofacial Surgeon, Faculty of Dentistry, Zahedan University of Medical Sciences, Zahedan, Iran
2Department of Oral Medicine, Faculty of Dentistry, Zahedan University of Medical Sciences, Zahedan, Iran
*Corresponding Author: Department of Oral Medicine, Faculty of Dentistry, Zahedan University of Medical Sciences, Zahedan, Iran Email: [email protected]

Zahedan Journal of Research in Medical Sciences:Vol. 15, issue 1; e93155
Published online:Apr 07, 2012
Article type:Case Report
Received:Feb 08, 2011
Accepted:Sep 15, 2011
How to Cite:Shirzaii M, Risbaf Fakour S. Gorlin Syndrome. Zahedan J Res Med Sci. 2013;15(1):e93155. doi:

Abstract

Gorlin syndrome is a dominant autosomal familial disorder. The manifestations begin at an early age and a combination of phenotypic abnormalities such special facial appearance, jaw cysts and skeletal anomalies are seen in this disease. A 22-year-old woman referred to Zahedan Dental School complaining of pain on the left cheek. During the examination, several cutaneous lesions in the neck, pits in palm and sole and multiple jaw cysts were observed. According to the clinical symptoms, lesion biopsy and reports of Gorlin syndrome radiography were presented.

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Copyright

© 2013, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.

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