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Gorlin Syndrome
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نویسنده
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Risbaf Siroos ,Shirzaii Masoomeh
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منبع
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zahedan journal of research in medical sciences - 2013 - دوره : 15 - شماره : 1 - صفحه:60 -62
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چکیده
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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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کلیدواژه
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Gorlin syndrome ,Basal cell carcinoma ,Jaw cyst
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آدرس
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zahedan university of medical sciences, Department of Oral Medicine, Faculty of Dentistry, Zahedan University of Medical Sciences, Zahedan, Iran, ایران, zahedan university of medical sciences, Department of Oral and Maxillofacial Surgeon, Faculty of Dentistry, Zahedan University of Medical Sciences, Zahedan, Iran, ایران
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پست الکترونیکی
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shirzaiy@gmail.com
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Authors
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