Clinical and Laboratory Investigation
Analysis of the KRT9 Gene in a Mexican Family with Epidermolytic Palmoplantar Keratoderma
Article first published online: 26 DEC 2012
© 2012 Wiley Periodicals, Inc.
Volume 30, Issue 3, pages 354–358, May/June 2013
How to Cite
Lopez-Valdez, J., Rivera-Vega, M. R., Gonzalez-Huerta, L. M., Cazarin, J. and Cuevas-Covarrubias, S. (2013), Analysis of the KRT9 Gene in a Mexican Family with Epidermolytic Palmoplantar Keratoderma. Pediatric Dermatology, 30: 354–358. doi: 10.1111/pde.12027
- Issue published online: 26 APR 2013
- Article first published online: 26 DEC 2012
Epidermolytic palmoplantar keratoderma (EPPK), an autosomal-dominant genodermatosis, is the most frequently occurring hereditary palmoplantar keratoderma. EPPK is characterized by hyperkeratosis of the palms and soles. Approximately 90% of patients present with mutations in the KRT9 gene, which encodes for keratin 9. Many of these mutations are located within the highly conserved coil 1A region of the alpha-helical rod domain of keratin 9, an important domain for keratin heterodimerization. The objective was to assess the clinical and molecular characteristics of a Mexican family with EPPK. The clinical characteristics of members of this family were analyzed. The KRT9 gene of affected members was polymerase chain reaction amplified from genomic DNA and sequenced. All affected members of the family had hyperkeratosis of the palms and soles with knuckle pads. The R163W mutation in the KRT9 gene was present in all affected individuals who were tested. Although R163W is the most frequent KRT9 mutation in patients with EPPK, only two families have been reported with knuckle pads associated with this mutation. Our findings indicate that knuckle pads can be associated with EPPK and the R163W mutation in a family with a genetic background different from that described here.