Papillon-Lefèvre Syndrome: A Series of Six Cases in the Same Family

Papillon-Lefèvre syndrome (PLS) is a rare, autosomal recessive heterogeneous disorder, which is characterized by palmoplantar hyperkeratosis, early loss of primary and permanent teeth, and associated calcification of the dura mater. Herein we described six cases of PLS in the same family. In this se...

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Detalles Bibliográficos
Autores principales: Kord Valeshabad, Ali, Mazidi, Abdolmotaleb, Kord Valeshabad, Reza, Imani, Elham, Kord, Hadi, Koohkan, Mohammad, Sayinar, Zrynal, Al-Talib, Khalil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scholarly Research Network 2012
Materias:
Clinical Study
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3518962/
https://www.ncbi.nlm.nih.gov/pubmed/23251811
http://dx.doi.org/10.5402/2012/139104

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3518962/
https://www.ncbi.nlm.nih.gov/pubmed/23251811
http://dx.doi.org/10.5402/2012/139104

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