Focal palmoplantar keratoderma with oral mucosal hyperkeratosis
- Focal palmoplantar keratoderma with oral mucosal hyperkeratosis
-
| Focal palmoplantar keratoderma with oral mucosal hyperkeratosis |
| Classification and external resources |
| OMIM |
114140 |
Focal palmoplantar keratoderma with oral mucosal hyperkeratosis (also known as "Focal epidermolytic palmoplantar keratoderma,"[1] "Hereditary painful callosities,"[2][1] "Hereditary painful callosity syndrome,"[3] "Keratosis follicularis,"[3] "Keratosis palmoplantaris nummularis"[3], and "Nummular epidermolytic palmoplantar keratoderma"[1]) is an autosomal dominant keratoderma that represents a clinical overlap syndrome with pachyonychia congenita type I but without the classic nail involvement.[3]:510
See also
References
- ^ a b c Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. pp. 785. ISBN 1-4160-2999-0.
- ^ Ryan P, Baird G, Benfanti P (March 2007). "Hereditary painful callosities: case report and review of the literature". Foot Ankle Int 28 (3): 377–8. doi:10.3113/FAI.2007.0377. PMID 17371662.
- ^ a b c d Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN 0071380760.
Categories:
- Genodermatoses
- Palmoplantar keratodermas
- Disease stubs
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