Papillon-Lefevre Syndrome: A Rare Case Report in Mongolia
Received Date: Jun 04, 2022 / Published Date: Jun 30, 2022
Abstract
Papillon-Lefèvre Syndrome (PLS) is a rare genetic disorder, characterized by Palmoplantar keratosis, aggressive periodontitis and premature edentulous primary and permanent dentition at a very young age. Additional symptoms and findings associated with PLS may include frequent pyogenic skin infections, abnormalities of the nails, and excessive perspiration. Papillon-Lefèvre syndrome is inherited in an autosomal recessive pattern. The various etiological and pathogenic factors are associated with the syndrome: immunologic alterations, genetic mutation and the role of the pathogenic microorganism. Dentists, especially pediatric dentist is very important specialist to diagnosis and management of PLS, there were the periodontal destruction at early childhood. We introduce the clinical presentation and management options of 5 years old boy with PLS in Mongolia.
Citation: Jargaltsogt D, Rashsuren O, Bayarsaikhan O, Altannamar M (2022) Papillon-Lefèvre Syndrome: A Rare Case Report in Mongolia. OMICS J Radiol 11: 386. Doi: 10.4172/2167-7964.1000386
Copyright: © 2022 Jargaltsogt D, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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