Papillon-Lefevre syndrome: A case report


Case Report

Author Details : Nilotpol Kashyap, Brij Kumar, Mukesh Kashyap, Dharmen Bhansali

Volume : 2, Issue : 4, Year : 2017

Article Page : 156-158


Suggest article by email

Get Permission

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.







View Article

PDF File  


Copyright permission

Get article permission for commercial use

Downlaod

PDF File    






Article Access statistics

Viewed: 1521

PDF Downloaded: 389