We report on a 22-year-old male patient and his father, both presenting with congenital sensorineural deafness, diffuse palmoplantar keratoderma and knuckle pads. These findings are similar to those previously described in the Bart-Pumphrey syndrome, a rare autosomal dominant disorder. Several conditions including keratoderma and deafness are briefly reviewed.
CITATION STYLE
de Oliveira, G. V., Steiner, C. E., Cintra, M. L., & Marques-de-Faria, A. P. (2003). Deafness, palmoplantar hyperkeratosis, and knuckle pads with male-to-male transmission: Bart-Pumphrey syndrome. Genetics and Molecular Biology. Brazilian Journal of Genetics. https://doi.org/10.1590/s1415-47572003000200004
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