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Papillon–Lefèvre syndrome: clinical presentation and management options
Papillon–Lefèvre syndrome (PLS) is a rare autosomal recessive disorder, characterized by diffuse palmoplantar keratoderma and precocious aggressive periodontitis, leading to premature loss of deciduous and permanent dentition at a very young age. Various etiopathogenic factors are associated with th...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4507741/ https://www.ncbi.nlm.nih.gov/pubmed/26203280 http://dx.doi.org/10.2147/CCIDE.S76080 |
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author | Sreeramulu, Basapogu Shyam, Naragani DVN Ajay, Pilla Suman, Pathipaka |
author_facet | Sreeramulu, Basapogu Shyam, Naragani DVN Ajay, Pilla Suman, Pathipaka |
author_sort | Sreeramulu, Basapogu |
collection | PubMed |
description | Papillon–Lefèvre syndrome (PLS) is a rare autosomal recessive disorder, characterized by diffuse palmoplantar keratoderma and precocious aggressive periodontitis, leading to premature loss of deciduous and permanent dentition at a very young age. Various etiopathogenic factors are associated with the syndrome, like immunologic alterations, genetic mutations, and the role of bacteria. Dentists play a significant 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. |
format | Online Article Text |
id | pubmed-4507741 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-45077412015-07-22 Papillon–Lefèvre syndrome: clinical presentation and management options Sreeramulu, Basapogu Shyam, Naragani DVN Ajay, Pilla Suman, Pathipaka Clin Cosmet Investig Dent Review Papillon–Lefèvre syndrome (PLS) is a rare autosomal recessive disorder, characterized by diffuse palmoplantar keratoderma and precocious aggressive periodontitis, leading to premature loss of deciduous and permanent dentition at a very young age. Various etiopathogenic factors are associated with the syndrome, like immunologic alterations, genetic mutations, and the role of bacteria. Dentists play a significant 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. Dove Medical Press 2015-07-15 /pmc/articles/PMC4507741/ /pubmed/26203280 http://dx.doi.org/10.2147/CCIDE.S76080 Text en © 2015 Sreeramulu et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Review Sreeramulu, Basapogu Shyam, Naragani DVN Ajay, Pilla Suman, Pathipaka Papillon–Lefèvre syndrome: clinical presentation and management options |
title | Papillon–Lefèvre syndrome: clinical presentation and management options |
title_full | Papillon–Lefèvre syndrome: clinical presentation and management options |
title_fullStr | Papillon–Lefèvre syndrome: clinical presentation and management options |
title_full_unstemmed | Papillon–Lefèvre syndrome: clinical presentation and management options |
title_short | Papillon–Lefèvre syndrome: clinical presentation and management options |
title_sort | papillon–lefèvre syndrome: clinical presentation and management options |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4507741/ https://www.ncbi.nlm.nih.gov/pubmed/26203280 http://dx.doi.org/10.2147/CCIDE.S76080 |
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