The prosthodontic management of a young edentulous patient with the papillon lefevre syndrome-a rare case report.
Identifieur interne : 000120 ( Ncbi/Merge ); précédent : 000119; suivant : 000121The prosthodontic management of a young edentulous patient with the papillon lefevre syndrome-a rare case report.
Auteurs : B. Sreeramulu [Inde] ; S. Haragopal ; K. Shalini ; Madhuri D. Sudha ; G. KiranSource :
- Journal of clinical and diagnostic research : JCDR [ 2249-782X ] ; 2012.
Abstract
The Papillon Lefevre syndrome is an autosomal recessive disorder which is characterized by various dermatological manifestations and periodontitis as a manifestation of a systemic disease. Its aetiopathogenesis is thought to be secondary to the mutation of the Cathepsin C gene. Various studies have shown that the immune related cells like the polymorphonuclear leucocytes and the macrophages and their precursors were affected.This report elicits about an edentulous male with this syndrome, who was treated with a modified complete denture prosthesis (hollow, maxillary, complete denture), considering his young age and low socioeconomic status.
DOI: 10.7860/JCDR/2012/4884.2607
PubMed: 23373060
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<front><div type="abstract" xml:lang="en">The Papillon Lefevre syndrome is an autosomal recessive disorder which is characterized by various dermatological manifestations and periodontitis as a manifestation of a systemic disease. Its aetiopathogenesis is thought to be secondary to the mutation of the Cathepsin C gene. Various studies have shown that the immune related cells like the polymorphonuclear leucocytes and the macrophages and their precursors were affected.This report elicits about an edentulous male with this syndrome, who was treated with a modified complete denture prosthesis (hollow, maxillary, complete denture), considering his young age and low socioeconomic status.</div>
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<Abstract><AbstractText>The Papillon Lefevre syndrome is an autosomal recessive disorder which is characterized by various dermatological manifestations and periodontitis as a manifestation of a systemic disease. Its aetiopathogenesis is thought to be secondary to the mutation of the Cathepsin C gene. Various studies have shown that the immune related cells like the polymorphonuclear leucocytes and the macrophages and their precursors were affected.This report elicits about an edentulous male with this syndrome, who was treated with a modified complete denture prosthesis (hollow, maxillary, complete denture), considering his young age and low socioeconomic status.</AbstractText>
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<CommentsCorrectionsList><CommentsCorrections RefType="Cites"><RefSource>J Clin Periodontol. 2000 Dec;27(12):951-4</RefSource>
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<CommentsCorrections RefType="Cites"><RefSource>J Indian Soc Pedod Prev Dent. 2002 Mar;20(1):9-11</RefSource>
<PMID Version="1">12435026</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Implant Dent. 2003;12(2):140-4</RefSource>
<PMID Version="1">12861881</PMID>
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<CommentsCorrections RefType="Cites"><RefSource>J Prosthet Dent. 1981 Apr;45(4):452-4</RefSource>
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<CommentsCorrections RefType="Cites"><RefSource>Implant Dent. 2010 Oct;19(5):394-9</RefSource>
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<CommentsCorrections RefType="Cites"><RefSource>J Periodontol. 1995 May;66(5):413-20</RefSource>
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<CommentsCorrections RefType="Cites"><RefSource>Int J Prosthodont. 2006 Jan-Feb;19(1):103-9</RefSource>
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<CommentsCorrections RefType="Cites"><RefSource>J Indian Soc Pedod Prev Dent. 2008 Jun;26(2):78-81</RefSource>
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<CommentsCorrections RefType="Cites"><RefSource>J Prosthet Dent. 1991 Jul;66(1):136-8</RefSource>
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