Papillon Lefèvre syndrome: A report of 3 cases with review of literature
Papillon Lefèvre syndrome (PLS) is a rare autosomal recessive disorder of keratinisation characterized by palmoplantar hyperkeratosis, periodontopathy and precocious (premature) loss of dentition. Exact mechanism of these clinical events mainly remains speculative. The periodontitis in PLS is usuall...
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Wolters Kluwer Medknow Publications
2008-01-01
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doaj-27aa3eb9111740c994350f4a85c156002020-11-24T23:51:22ZengWolters Kluwer Medknow PublicationsJournal of Indian Academy of Oral Medicine and Radiology0972-13630975-15722008-01-01201364010.4103/0972-1363.44360Papillon Lefèvre syndrome: A report of 3 cases with review of literatureAnita MundeManjiri JoshiSonia SagooSafia ShoebPapillon Lefèvre syndrome (PLS) is a rare autosomal recessive disorder of keratinisation characterized by palmoplantar hyperkeratosis, periodontopathy and precocious (premature) loss of dentition. Exact mechanism of these clinical events mainly remains speculative. The periodontitis in PLS is usually difficult to control. Effective treatment includes extraction of primary teeth combined with oral antibiotics and professional teeth cleaning. Dentists play a significant role in the diagnosis and management of PLS patients. This paper describes 3 cases of PLS reporting to the out patient department within a span of 2 years with classic clinical features and briefly reviews the literature.http://www.jiaomr.in/article.asp?issn=0972-1363;year=2008;volume=20;issue=1;spage=36;epage=40;aulast=MundePalmoplantar hyperkeratosispapillon Lefèvre syndrome and periodontitis |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Anita Munde Manjiri Joshi Sonia Sagoo Safia Shoeb |
spellingShingle |
Anita Munde Manjiri Joshi Sonia Sagoo Safia Shoeb Papillon Lefèvre syndrome: A report of 3 cases with review of literature Journal of Indian Academy of Oral Medicine and Radiology Palmoplantar hyperkeratosis papillon Lefèvre syndrome and periodontitis |
author_facet |
Anita Munde Manjiri Joshi Sonia Sagoo Safia Shoeb |
author_sort |
Anita Munde |
title |
Papillon Lefèvre syndrome: A report of 3 cases with review of literature |
title_short |
Papillon Lefèvre syndrome: A report of 3 cases with review of literature |
title_full |
Papillon Lefèvre syndrome: A report of 3 cases with review of literature |
title_fullStr |
Papillon Lefèvre syndrome: A report of 3 cases with review of literature |
title_full_unstemmed |
Papillon Lefèvre syndrome: A report of 3 cases with review of literature |
title_sort |
papillon lefèvre syndrome: a report of 3 cases with review of literature |
publisher |
Wolters Kluwer Medknow Publications |
series |
Journal of Indian Academy of Oral Medicine and Radiology |
issn |
0972-1363 0975-1572 |
publishDate |
2008-01-01 |
description |
Papillon Lefèvre syndrome (PLS) is a rare autosomal recessive disorder of keratinisation characterized by palmoplantar hyperkeratosis, periodontopathy and precocious (premature) loss of dentition. Exact mechanism of these clinical events mainly remains speculative. The periodontitis in PLS is usually difficult to control. Effective treatment includes extraction of primary teeth combined with oral antibiotics and professional teeth cleaning. Dentists play a significant role in the diagnosis and management of PLS patients. This paper describes 3 cases of PLS reporting to the out patient department within a span of 2 years with classic clinical features and briefly reviews the literature. |
topic |
Palmoplantar hyperkeratosis papillon Lefèvre syndrome and periodontitis |
url |
http://www.jiaomr.in/article.asp?issn=0972-1363;year=2008;volume=20;issue=1;spage=36;epage=40;aulast=Munde |
work_keys_str_mv |
AT anitamunde papillonlefevresyndromeareportof3caseswithreviewofliterature AT manjirijoshi papillonlefevresyndromeareportof3caseswithreviewofliterature AT soniasagoo papillonlefevresyndromeareportof3caseswithreviewofliterature AT safiashoeb papillonlefevresyndromeareportof3caseswithreviewofliterature |
_version_ |
1725476062098358272 |