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GORLIN-GOLTZ SYNDROME
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نویسنده
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Pakfetrat Atessa ,Falaki Farnaz ,Mahmoodabadi Reza Zare ,Saghafi Shadi
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منبع
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pakistan journal of medical sciences - 2010 - دوره : 26 - شماره : 1 - صفحه:235 -238
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چکیده
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We report a case of gorlin-goltz syndrome in a 21-year-old man. gorlin-goltz syndrome (basal cell nevus syndrome) is an infrequent hereditary disease with its prevalence varying from 1/ 57,000 to 1/250,000.it is principally characterized by a wide range of developmental abnormalities. main clinical manifestations include multiple odontogenic keratocysts of the jaws, facial basal cell carcinomas and skeletal anomalies. the prevalence varies from 1/57,000 to 1/250,000.
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کلیدواژه
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Gorlin-Goltz Syndrome ,Nevoid Basal Cell Carcinoma Syndrome (NBCCS) ,Basal Cell Nevus Syndrome ,Odontogenic Keratocyst ,Basal Cell Carcinoma
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آدرس
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mashhad university of medical sciences, Faculty of Dentistry, Dental Research Center, ایران, mashhad university of medical sciences, Faculty of Dentistry, Dental Research Center, ایران, mashhad university of medical sciences, Faculty of Dentistry, Dental Research Center, ایران, mashhad university of medical sciences, Faculty of Dentistry, Dental Research Center, ایران
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پست الکترونیکی
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falakif@mums.ac.ir,farnazfalaki@yahoo.com
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Authors
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