Epidermolytic Hyperkeratosis – A rare case report.
dc.contributor.author | Kataria, Usha | |
dc.contributor.author | Chhillar, Dinesh | |
dc.contributor.author | Dhattarwal, S K | |
dc.date.accessioned | 2015-10-23T07:27:47Z | |
dc.date.available | 2015-10-23T07:27:47Z | |
dc.date.issued | 2015-06 | |
dc.description.abstract | A 20 year old boy presented to the dermatology department for treatment of a congenital icthyosis with a history of generalized erythroderma and trauma related blistering since birth. At the time of presentation he was noted to have red hyperkeratotic plaques all over the body. Lesions were corrugated over the joint flexures, elbows, knees, and dorsal of hands. In the subsequent months after birth erythema and blistering improved but patient developed hyperkeratotic scaling that was especially prominent over the joint flexures neck, hands and feet. Treatment options include urea or alpha-hydroxy acid containing creams as well as topical and systemic retinoids. | en_US |
dc.identifier.citation | Kataria Usha, Chhillar Dinesh, Dhattarwal S K. Epidermolytic Hyperkeratosis – A rare case report. International Archives of Integrated Medicine. 2015 Jun; 2(6): 232-235. | en_US |
dc.identifier.issn | 2394-0026 (P) | |
dc.identifier.issn | 2394-0034 (O) | |
dc.identifier.uri | https://imsear.searo.who.int/handle/123456789/164768 | |
dc.language.iso | en | en_US |
dc.source.uri | https://iaimjournal.com/wp-content/uploads/2015/06/iaim_2015_0206_32.pdf | en_US |
dc.subject | Hyperkeratosis | en_US |
dc.subject | Erythroderma | en_US |
dc.subject | Congential | en_US |
dc.subject | Trauma related blister | en_US |
dc.title | Epidermolytic Hyperkeratosis – A rare case report. | en_US |
dc.type | Article | en_US |