H00755 | |
H number | H00755 |
Name | Acrokeratosis verruciformis |
Description | Acrokeratosis verruciformis is a rare autosomal dominant genodermatosis characterized by multiple planar wart-like lesions on the hands and feet. The lesions are usually present at birth. Mutations in ATP2A2 encoding the calcium pump in sarcoendoplasmic reticulum have been identified. |
Category | Congenital malformation |
Network | - |
Gene | ATP2A2 [HSA:488] [KO:K05853] |
Pathogen | - |
Env factor | - |
Carcinogen | - |
Drug | - |
Comment | - |
Other DBs | ICD-11: EC20.Y ICD-10: Q82.8 MeSH: D007644 OMIM: 101900 |
Reference | PMID:12542527 AUTHORS Dhitavat J, Macfarlane S, Dode L, Leslie N, Sakuntabhai A, MacSween R, Saihan E, Hovnanian A TITLE Acrokeratosis verruciformis of Hopf is caused by mutation in ATP2A2: evidence that it is allelic to Darier's disease. JOURNAL J Invest Dermatol 120:229-32 (2003) DOI:10.1046/j.1523-1747.2003.t01-1-12045.x PMID:22028575 AUTHORS Bang CH, Kim HS, Park YM, Kim HO, Lee JY TITLE Non-familial Acrokeratosis Verruciformis of Hopf. JOURNAL Ann Dermatol 23 Suppl 1:S61-3 (2011) DOI:10.5021/ad.2011.23.S1.S61 PMID:16150218 AUTHORS Rallis E, Economidi A, Papadakis P, Verros C TITLE Acrokeratosis verruciformis of Hopf (Hopf disease): case report and review of the literature. JOURNAL Dermatol Online J 11:10 (2005) |