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.
Translated title of the contribution | The Papillon-Lefèvre syndrome. A clinical and ultrastructural study of 2 cases |
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Original language | Italian |
Pages (from-to) | 433-441 |
Number of pages | 9 |
Journal | Minerva Stomatologica |
Volume | 47 |
Issue number | 9 |
Publication status | Published - 1998 |