Síndrome de Papillon-Lefèvre.

BACKGROUND: Papillon-Lefevre syndrome is an autosomal recessive type IV genodermatosis, it is estimated that 1-4 per million inhabitants are affected and it is associated in 20-40% of cases with consanguinity. It is due to a mutation in the gene that encodes cathepsin C and is characterized by palmo...

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Bibliographic Details

Published in:	Dermatología Revista Mexicana Vol. 69; no. 6; pp. 838 - 846
Main Authors:	Staines Boone, Aidé Tamara, Pérez Arroyo, Martha Viridiana, Navarrete Solís, Josefina, Sánchez Alva, María Eugenia Karina, González Cabello, Diana, Boone Barrera, Erika A., Ugalde Trejo, Nora Ximena, Delgado Moreno, Karla Paola
Format:	Article
Published:	Edicion y Farmacia S.A. de C.V. nov/dic2025
Subjects:	Periodontitis Palmoplantar keratoderma Genetic mutation Quality of life Disease relapse Family history (Medicine) Skin diseases
Online Access:	View this record in EBSCOhost