Gorlin Syndrome in Eleven Patients

Gorlin Syndrome in Eleven Patients

Aim: Gorlin syndrome is an autosomal dominant disorder characterized by cutaneous basal cell carcinomas, odontogenic keratocysts and skeletal anomalies. Predisposition to certain types of cancers is among the main features of the disease. Chromosome instability was suspected as a mechanism for cance...

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Bibliographic Details
Main Authors: Gülen Eda Utine, Yasemin Alanay, Dilek Aktaş, Koray Boduroğlu, Mehmet Alikaşifoğlu, Ergül Tunçbilek
Format: Article
Language:English
Published: Galenos Yayinevi 2017-06-01
Series:Journal of Pediatric Research
Subjects:
Gorlin syndrome
hairy patch
chromosome instability
sister chromatid exchange
hypopigmented lesion
Online Access:http://jpedres.org/article_15022/Gorlin-Syndrome-In-Eleven-Patients

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http://jpedres.org/article_15022/Gorlin-Syndrome-In-Eleven-Patients

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