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Initial expression of the Papillon-Lefevre syndrome in consanguine family.
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Papillon-Lefèvre syndrome: neutrophil function in 15 cases fron 4 families in Egypt.
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Papillon-Lefevre syndrome-like presentation in chronic arsenicosis: A rare mimicry.
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本文引用的文献

1
Diagnosis of Papillon-Lefèvre syndrome: review of the literature and a case report.
Postepy Dermatol Alergol. 2020 Oct;37(5):671-676. doi: 10.5114/ada.2020.100480. Epub 2020 Nov 7.
2
Papillon-Lefèvre syndrome: a series of five cases among siblings.
J Med Case Rep. 2016 Sep 22;10(1):260. doi: 10.1186/s13256-016-1051-z.
3
Characterization of neutrophil function in Papillon-Lefèvre syndrome.
J Leukoc Biol. 2016 Aug;100(2):433-44. doi: 10.1189/jlb.5A1015-489R. Epub 2016 Mar 8.
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Papillon-Lefèvre syndrome: clinical presentation and management options.
Clin Cosmet Investig Dent. 2015 Jul 15;7:75-81. doi: 10.2147/CCIDE.S76080. eCollection 2015.
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Median nail damage in nail-patella syndrome associated with triangular lunulae.
Br J Dermatol. 2015 Dec;173(6):1559-61. doi: 10.1111/bjd.13942. Epub 2015 Oct 30.
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Nail-Patella Syndrome: clinical and molecular data in 55 families raising the hypothesis of a genetic heterogeneity.
Eur J Hum Genet. 2016 Jan;24(1):44-50. doi: 10.1038/ejhg.2015.77. Epub 2015 Apr 22.
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Papillon-Lefevre syndrome: Reporting consanguinity as a risk factor.
Saudi Dent J. 2014 Jul;26(3):126-31. doi: 10.1016/j.sdentj.2014.02.004. Epub 2014 Apr 19.
9
Dermatologic and oral findings in a cohort of 47 patients with Papillon-Lefèvre syndrome.
J Am Acad Dermatol. 2003 Mar;48(3):345-51. doi: 10.1067/mjd.2003.197.
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Haim-Munk syndrome and Papillon-Lefèvre syndrome are allelic mutations in cathepsin C.
J Med Genet. 2000 Feb;37(2):88-94. doi: 10.1136/jmg.37.2.88.

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