Acrokeratosis verruciformis
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Acrokeratosis verruciformis
| Acrokeratosis verruciformis | |
|---|---|
| Classification and external resources | |
| OMIM | 101900 |
| DiseasesDB | 3467 |
| eMedicine | article/1055892 |
| 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
References
- ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 1-4160-2999-0.
- ^ Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN 0-07-138076-0.
- ^ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0-7216-2921-0.
- ^ 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. doi:10.1046/j.1523-1747.2003.t01-1-12045.x. PMID 12542527.
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