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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Kord Valeshabad, Ali, Mazidi, Abdolmotaleb, Kord Valeshabad, Reza, Imani, Elham, Kord, Hadi, Koohkan, Mohammad, Sayinar, Zrynal, Al-Talib, Khalil
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: International Scholarly Research Network 2012
Pynciau:
Clinical Study
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC3518962/
https://ncbi.nlm.nih.gov/pubmed/23251811
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5402/2012/139104
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