Epidermolytic Hyperkeratosis – A rare case report.

dc.contributor.authorKataria, Usha
dc.contributor.authorChhillar, Dinesh
dc.contributor.authorDhattarwal, S K
dc.date.accessioned2015-10-23T07:27:47Z
dc.date.available2015-10-23T07:27:47Z
dc.date.issued2015-06
dc.description.abstractA 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.citationKataria 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.issn2394-0026 (P)
dc.identifier.issn2394-0034 (O)
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/164768
dc.language.isoenen_US
dc.source.urihttps://iaimjournal.com/wp-content/uploads/2015/06/iaim_2015_0206_32.pdfen_US
dc.subjectHyperkeratosisen_US
dc.subjectErythrodermaen_US
dc.subjectCongentialen_US
dc.subjectTrauma related blisteren_US
dc.titleEpidermolytic Hyperkeratosis – A rare case report.en_US
dc.typeArticleen_US
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