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Papillon–Lefevre syndrome: Reporting consanguinity as a risk factor
Papillon–Lefevre syndrome (PLS) is an autosomal recessive genetic disorder characterized by palmoplantar hyperkeratosis associated with severe early-onset periodontitis and premature loss of primary and permanent teeth. This report describes two cases of PLS in 28-year-old female and 16-year-old mal...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elsevier
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4095039/ https://ncbi.nlm.nih.gov/pubmed/25057233 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.sdentj.2014.02.004 |
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