Al-Dhubaibi, Mohammed and Metwaly, Hamdy and Elkarargy, Amr (2016) Paillion- Lefèvere Syndrome: A Case Report. British Journal of Medicine and Medical Research, 13 (9). pp. 1-5. ISSN 22310614
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Abstract
Papillon-Lefèvere Syndrome (PLS) is one of the rare autosomal recessive disorders of keratinization (1-4 cases per million). It is inherited as an autosomal-recessive condition with one-third of the patients showing consanguinity of the parents and diagnosed in both sexes. Lesions are characterized by palmo-plantar hyperkeratosis and severe destructive periodontal disease affecting the primary and permanent teeth. This paper reports a case of a 13 -year-old African boy presented to the outpatient clinic of Qassim University with diffuse keratotic plaques of his soles extending to the dorsal surface, localized keratotic plaques of his palm and severe inflammation of the gingiva with premature teeth loss and looseness of remaining teeth.
Item Type: | Article |
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Subjects: | ArticleGate > Medical Science |
Depositing User: | Managing Editor |
Date Deposited: | 26 May 2023 05:06 |
Last Modified: | 08 Jun 2024 09:38 |
URI: | http://ebooks.pubstmlibrary.com/id/eprint/2851 |