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[The Papillon-Lefèvre syndrome. A clinical and ultrastructural study of 2 cases].

Identifieur interne : 009E32 ( Ncbi/Checkpoint ); précédent : 009E31; suivant : 009E33

[The Papillon-Lefèvre syndrome. A clinical and ultrastructural study of 2 cases].

Auteurs : R. Antoni ; E. Accivile ; G A Perrone ; M A Russo

Source :

RBID : pubmed:9835752

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English descriptors

Abstract

Two cases of Papillon-Lefèvre syndrome, a rare hereditary affection of unknown etiology, whose clinical signs are hyperkeratosis palmoplantaris and parodontitis, are described. The results obtained with the ultrastructural examination of the lesions are shown. A therapeutic protocol which can reduce the evolution of the pathology, is also suggested.

PubMed: 9835752


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pubmed:9835752

Le document en format XML

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<term>Foot (pathology)</term>
<term>Gingiva (ultrastructure)</term>
<term>Hand (pathology)</term>
<term>Humans</term>
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<term>Femelle</term>
<term>Gencive (ultrastructure)</term>
<term>Humains</term>
<term>Main (anatomopathologie)</term>
<term>Maladie de Papillon-Lefèvre ()</term>
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<term>Mobilité dentaire (anatomopathologie)</term>
<term>Mâle</term>
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<term>Papillon-Lefevre Disease</term>
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<term>Maladie de Papillon-Lefèvre</term>
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<div type="abstract" xml:lang="en">Two cases of Papillon-Lefèvre syndrome, a rare hereditary affection of unknown etiology, whose clinical signs are hyperkeratosis palmoplantaris and parodontitis, are described. The results obtained with the ultrastructural examination of the lesions are shown. A therapeutic protocol which can reduce the evolution of the pathology, is also suggested.</div>
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