Gorlin Syndrome

Author	Masoomeh Shirzaii	en
Author	Sirous Risbaf Fakour	en
Issued Date	2013-01-31	en
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.	en
DOI	https://doi.org/	en
Keyword	Gorlin syndrome	en
Keyword	Basal cell carcinoma	en
Keyword	Jaw cyst	en
Publisher	Brieflands	en
Title	Gorlin Syndrome	en
Type	Case Report	en

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