Title:
Familial pityriasis rubra pilaris: A case report

dc.contributor.authorManish Bansal
dc.contributor.authorKajal Manchanda
dc.contributor.authorAnurag
dc.contributor.authorS.S. Pandey
dc.date.accessioned2026-02-07T05:43:35Z
dc.date.issued2013
dc.description.abstractPityriasis rubra pilaris (PRP) is a rare papulosquamous disorder of unknown etiology characterized by reddish orange plaques with pityriasiform scaling with follicular keratoses, palmoplantar keratoderma, and occasionally erythroderma. We hereby report a family with five members affected with the condition in three successive generations.
dc.identifier.issn15609014
dc.identifier.urihttps://dl.bhu.ac.in/bhuir/handle/123456789/25645
dc.subjectAcitretin
dc.subjectFamilial
dc.subjectPityriasis rubra pilaris
dc.titleFamilial pityriasis rubra pilaris: A case report
dc.typePublication
dspace.entity.typeArticle

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