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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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| Gepubliceerd in: | J Med Case Rep |
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| Hoofdauteurs: | , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
BioMed Central
2016
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| Onderwerpen: | |
| Online toegang: | 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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