Publication:
Sporadic Progressive Symmetric Erythrokeratoderma: Classical Presentation of a rare Condition

creativeworkseries.issnISSN 2091-0231 eISSN 2091-167X
dc.contributor.authorAgarwal, Kompal
dc.contributor.authorAgrawal, Sudha
dc.contributor.authorPradhan, Anju
dc.date.accessioned2025-08-25T08:01:38Z
dc.date.available2025-08-25T08:01:38Z
dc.date.issued2019
dc.descriptionKompal Agarwal BP Koirala Institute of Health Sciences Sudha Agrawal BP Koirala Institute of Health Sciences, Dharan Anju Pradhan BP Koirala Institute of Health Sciences, Dharan
dc.description.abstractAbstract: Progressive symmetrical erythrokeratodermia (PSEK) is a rare autosomal dominant genodermatosis presenting in infancy or early childhood. An 11-year-old male presented with a history of pruritic, erythematous, scaly, hyperkeratotic plaques first noted at 5 years of age, with no history of similar lesions in the family. Cutaneous examination revealed multiple, irregularly shaped, erythematous plaques with fine, shiny white, adherent scaling distributed symmetrically over the face, trunk, inguinal area, bilateral axillae and extensor surfaces of limbs. Palmoplantar keratoderma was present with thickened, yellowish discolored nails. No systemic abnormality was found. The histopathological findings were consistent with PSEK. The case is being reported to increase the awareness about this rare disease. Keywords: Genetic Heterogeneity, Keratoderma, palmoplantar, Nepal, Retinoids
dc.identifierhttps://doi.org/10.3126/njdvl.v17i1.23293
dc.identifier.urihttps://hdl.handle.net/20.500.14572/2020
dc.language.isoen_US
dc.publisherSociety of Dermatologists, Venereologists and Leprologists of Nepal (SODVELON)
dc.titleSporadic Progressive Symmetric Erythrokeratoderma: Classical Presentation of a rare Condition
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage72
oaire.citation.startPage69
relation.isJournalIssueOfPublication4961346d-d09b-46c9-b0e0-f7ec90484ad6
relation.isJournalIssueOfPublication.latestForDiscovery4961346d-d09b-46c9-b0e0-f7ec90484ad6
relation.isJournalOfPublicationb2ab7aab-75b0-4bd1-9ed0-b8a91c68201a

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