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Acrokeratosis verruciformis

Acrokeratosis verruciformis
Classification and external resources
ICD-10 Q82.8
OMIM 101900
DiseasesDB 3467
eMedicine article/1055892
NCI Acrokeratosis verruciformis
Patient UK Acrokeratosis verruciformis
MeSH D007644

Acrokeratosis verruciformis (also known as "Acrokeratosis verruciformis of Hopf"[1]:1666) is a rare autosomal dominant disorder appearing at birth or in early childhood, characterized by skin lesions that are small, verrucous, flat papules resembling warts.[2]:527[3]:568

Like Darier's disease, it is associated with ATP2A2.[4]

See also


  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 0-07-138076-0.
  3. James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0-7216-2921-0.
  4. Dhitavat J, Macfarlane S, Dode L et al. (February 2003). "Acrokeratosis verruciformis of Hopf is caused by mutation in ATP2A2: evidence that it is allelic to Darier's disease". J. Invest. Dermatol. 120 (2): 229–32. PMID 12542527. doi:10.1046/j.1523-1747.2003.t01-1-12045.x. 

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