Síndrome de Papillón-Lefévre. Hiperqueratosis palmo-plantar y enfermedad periodontal agresiva. Caso clínico
Wedi'i Gadw mewn:
| Awdur: | |
|---|---|
| Fformat: | artículo original |
| Statws: | Versión publicada |
| Dyddiad Cyhoeddi: | 2012 |
| Disgrifiad: | The Papillon-Lefévre Syndrome is a rare syndrome that appears in 1 to 4 live births per millon. It is characterized by erythematous palmoplantar hyperkeratosis and agresive periodontal disease that affect both dentition and lead to the total loss of teeth at an in early age. The present article refers to the diagnosis of the syndrome in four sisters residents of Llano Grande de Cartago, the initial treatment took place at the Center of Specialities of Dentistry and Dermatology in the Calderon Guardia Hospital. The early identification of the syndrome plays an important role in prolonging the permanency of the teeth for a longer period in the oral cavity. |
| Gwlad: | Portal de Revistas UCR |
| Sefydliad: | Universidad de Costa Rica |
| Repositorio: | Portal de Revistas UCR |
| Iaith: | Español |
| OAI Identifier: | oai:archivo.portal.ucr.ac.cr:article/4768 |
| Mynediad Ar-lein: | https://archivo.revistas.ucr.ac.cr/index.php/Odontos/article/view/4768 |
| Allweddair: | Papillon-Lefevre Syndrome - Periodontal disease - palmoplantar hyperkeratosis – quimiotaxis - catepsin C |