Scleroatrophic syndrome of Huriez

Scleroatrophic syndrome of Huriez
Classification and external resources
OMIM 181600
DiseasesDB 32828

Scleroatrophic syndrome of Huriez (also known as "Huriez syndrome," "Palmoplantar keratoderma with scleroatrophy,"[1] "Palmoplantar keratoderma with sclerodactyly," "Scleroatrophic and keratotic dermatosis of the limbs," and "Sclerotylosis") is an autosomal dominant keratoderma with sclerodactyly present at birth with a diffuse symmetric keratoderma of the palms and soles.[2]:513[3]:576

An association with 4q23 has been described. [4]

It was characterized in 1968.[5]

See also

References

  1. ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 1-4160-2999-0. 
  2. ^ Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN 0071380760.
  3. ^ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0721629210.
  4. ^ Lee YA, Stevens HP, Delaporte E, Wahn U, Reis A (January 2000). "A gene for an autosomal dominant scleroatrophic syndrome predisposing to skin cancer (Huriez syndrome) maps to chromosome 4q23". Am. J. Hum. Genet. 66 (1): 326–30. doi:10.1086/302718. PMC 1288338. PMID 10631162. http://linkinghub.elsevier.com/retrieve/pii/S0002-9297(07)62258-7. 
  5. ^ Huriez C, Deminatti M, Agache P, Menecier F (1968). "[Une genodysplasie non encore individualisee: la genodermatose sclero-atrophiante et keratodermique des extremites frequemment degenerative.]" (in French). Sem. Hop. Paris, 1968 44 (6): 481–488. PMID 4298032.