A family with palmoplantar epidermolytic hyperkeratosis
- 1 July 1989
- journal article
- case report
- Published by Oxford University Press (OUP) in Clinical and Experimental Dermatology
- Vol. 14 (4) , 313-316
- https://doi.org/10.1111/j.1365-2230.1989.tb01991.x
Abstract
Familial epidermolytic hyperkeratosis confined to the palms and soles was first characterized by Klaus and Weinstein in 1970. This entity has been the subject of only four subsequent reports. We report a family previously diagnosed as suffering from tylosis (Thost Unna syndrome), in which eleven members have been affected, and review the literature on this disease. It would seem possible that this entity may be more common than the sparse literature would indicate, and that other cases may currently be masquerading as tylosis.Keywords
This publication has 5 references indexed in Scilit:
- Epidermolytic hereditary palmoplantar keratoderma.British Journal of Dermatology, 1978
- Familial Congenital Epidermolytic Hyperkeratosis Confined to the Palms and SolesSouthern Medical Journal, 1974
- Localized Epidermolytic HyperkeratosisArchives of Dermatology, 1970
- Variations of Congenital Ichthyosiform ErythrodermaArchives of Dermatology, 1965