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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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| Publicado no: | J Med Case Rep |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5034476/ https://ncbi.nlm.nih.gov/pubmed/27658951 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13256-016-1051-z |
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