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

  1. ^ 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. 
  2. ^ 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. 
  3. ^ a b c d Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN 0071380760.