Case Report
Author Details :
Volume : 2, Issue : 4, Year : 2017
Article Page : 156-158
Abstract
Papillon–Lefèvre syndrome (PLS) is a rare autosomal recessive disorder which is characterized by diffuse palmoplantar keratoderma and precocious aggressive periodontitis, resulting in premature loss of deciduous and permanent dentition at a very early age. Several etiopathogenic factors are responsible for the syndrome, like immunologic alterations, genetic mutations, and also the role of microorganisms. Dentists play a major role in the diagnosis and management of PLS as there are characteristic manifestations like periodontal destruction at an early age and an early eruption of permanent teeth. Here, we are presenting an elaborate review of PLS, its etiopathogenesis, clinical presentation, and management options.
Keywords: Periodontitis, Modified Complete Dentures, Primary and Permanent dentition, Palmoplantar Keratoderma.
How to cite : Kashyap N, Kumar B, Kashyap M, Bhansali D, Papillon-Lefevre syndrome: A case report. IP Int J Periodontol Implantol 2017;2(4):156-158
This is an Open Access (OA) journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
Viewed: 1521
PDF Downloaded: 389