Síndrome de Papillón- Lefévre. Hiperqueratosis palmo-plantar y enfermedad periodontal agresiva. Caso clínico.

dc.creator	Morales Vargas, Milton
dc.date	2012-02-01
dc.date.accessioned	2016-05-02T22:19:09Z
dc.date.available	2016-05-02T22:19:09Z
dc.identifier	http://revistas.ucr.ac.cr/index.php/Odontos/article/view/4768
dc.identifier.uri	https://hdl.handle.net/10669/21364
dc.description	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.	es-ES
dc.format	application/pdf
dc.language	spa
dc.publisher	Universidad de Costa Rica	en-US
dc.rights	Copyright (c) 2014 Odovtos	en-US
dc.source	Odovtos International Journal of Dental Sciences; No 13 (2011): Odovtos:No. 13 -2011; 42-47	es-ES
dc.source	Odovtos - International Journal of Dental Sciences; No 13 (2011): Odovtos:No. 13 -2011; 42-47	en-US
dc.source	2215-3411
dc.source	1659-1046
dc.source	10.15517/ijds.v0i13
dc.title	Síndrome de Papillón- Lefévre. Hiperqueratosis palmo-plantar y enfermedad periodontal agresiva. Caso clínico.	es-ES
dc.type	artículo original
dc.coverage	CRC	es-ES

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