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Papillon-Lefevre Disease

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Recent Publications on Papillon-Lefevre Disease:

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HLA class I gene polymorphism in Iranian patients with Papillon-Lefevre Syndrome.
BACKGROUND: Papillon-Lefevre Syndrome (PLS) is a rare autosomal recessive...
9th April, 2008
Department of Immunology, School of Medicine, Shiraz University of Medical Iran J Immunol. 2007 Dec;4(4):241-5.
DOI Direct Link
Functional Cathepsin C mutations cause different Papillon-Lefevre syndrome phenotypes.
AIM: The autosomal-recessive Papillon-Lefevre syndrome (PLS) is...
1st April, 2008
Department of Conservative Dentistry, University Hospital Carl Gustav J Clin Periodontol. 2008 Apr;35(4):311-6. Epub 2008 Feb 20.
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Detection of an intragenic deletion expands the spectrum of CTSC mutations in Papillon-Lefevre syndrome.
The Papillon-Lefevre syndrome (PLS) is an autosomal recessive disorder....
20th February, 2008
Departement de Dermatologie, Hopital Saint Andre, Bordeaux, France. J Invest Dermatol. 2008 Feb;128(2):322-5. Epub 2007 Oct 18.
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Dermatologic, periodontal, and skeletal manifestations of Haim-Munk syndrome in two siblings.
Haim-Munk syndrome is an extremely rare autosomal recessive disorder of...
9th February, 2008
Ayza Skin and Research Center, Lalamusa, Pakistan. J Am Acad Dermatol. 2008 Feb;58(2):339-44.
DOI Direct Link
Acitretin for Papillon-Lefevre syndrome in a five-year-old girl.
Haim-Munk syndrome is an extremely rare autosomal recessive disorder of...
8th February, 2008
Indian J Dermatol Venereol Leprol. 2008 Jan-Feb;74(1):71-3.

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Wikipedia excerpt, where present, licenced under the GNU Free Documentation License. Resources from the NCBI applied. Selected MeSH subject headings created and maintained by the US NLM are used in conjunction with additional keywords. 2006-2008 MeSH.
 

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