Papillon–Lefèvre syndrome: a series of five cases among siblings

BACKGROUND: Papillon–Lefèvre syndrome is a rare autosomal recessive disorder characterized by palmoplantar hyperkeratosis and aggressively progressing periodontitis leading to premature loss of deciduous and permanent dentition. The etiopathogenesis of the syndrome is relatively obscure, and immunol...

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Detalles Bibliográficos
Autores principales: AIBarrak, Zyad M., Alqarni, Adel S., Chalisserry, Elna P., Anil, Sukumaran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5034476/
https://www.ncbi.nlm.nih.gov/pubmed/27658951
http://dx.doi.org/10.1186/s13256-016-1051-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5034476/
https://www.ncbi.nlm.nih.gov/pubmed/27658951
http://dx.doi.org/10.1186/s13256-016-1051-z

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