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 |
|---|---|
| Original language | Italian |
| Pages (from-to) | 433-441 |
| Number of pages | 9 |
| Journal | Minerva Stomatologica |
| Volume | 47 |
| Issue number | 9 |
| Publication status | Published - 1998 |
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Antoni, R., Accivile, E., Perrone, G. A., & Russo, M. A. (1998). Sindrome di Papillon-Lefèvre. Studio clinico e ultrastrutturale su due casi. Minerva Stomatologica, 47(9), 433-441.