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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Hlavní autoři: Shah, Aasim Farooq, Tangade, Pradeep, Agarwal, Swatantra
Médium: Artigo
Jazyk:Inglês
Vydáno: Elsevier 2014
Témata:
Case Report
On-line přístup: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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