@ARTICLE{Basirat, author = {Basirat, Maryam and Pakfetrat, Atessa and Javadian Langaroodi, Adineh and }, title = {Papillon-Lefèvre Syndrome: a case report}, volume = {1}, number = {2}, abstract ={Introduction: Papillon-Lefèvre syndrome(PLS) characterized by palmoplantar hyperkeratosis is a rare autosomal recessive genetic disorder with rapidly progressive periodontitis and premature loss of both deciduous and permanent teeth. In this study, we report the clinical and radiographic features of Papillon-Lefèvre syndrome in an 11- year-old girl and we also discuss the history and various theories about the etiology and treat‌ment planning for this syndrome. }, URL = {http://3dj.gums.ac.ir/article-1-34-en.html}, eprint = {http://3dj.gums.ac.ir/article-1-34-en.pdf}, journal = {Journal title}, doi = {10.18869/acadpub.3dj.1.2.33}, year = {2012} }