Abstract
Papillon-Lefevre syndrome is a very rare autosomal recessive condition characterised by pronounced palmoplantar hyperkeratosis and severe early onset periodontitis, leading to early loss of teeth. Here, we report a case of Papillon-Lefevre syndrome with a brief discussion on treatment aspect.
Article Type
Case Report
First Page
941
Last Page
943
Recommended Citation
Thomas, Shibu; Gummadapu, Sarat; Ahsan, Auswaf; and Pai, Keerthilatha M.
(2004)
"Papillon Lefevre syndrome,"
Saudi Medical Journal: Vol. 25:
Iss.
7, Article 23.
DOI: https://doi.org/10.15537/1658-3175.2480