Publication:
Cyclosporine-Induced Alopecia in Childhood Nephrotic Syndrome – A Case Report

creativeworkseries.issnISSN 1990-7974 eISSN 1990-7982
dc.contributor.authorNaj, Mohsina
dc.contributor.authorSk, Md Habibullah
dc.date.accessioned2025-10-14T09:30:56Z
dc.date.available2025-10-14T09:30:56Z
dc.date.issued2024
dc.descriptionMohsina Naj MD Paediatrics, Post Doctoral Trainee, Department of Nephrology, Institute of Post Graduate Medical Education & Research and SSKM Hospital, 244, A J C Bose Road, Kolkata-700020, India. Md Habibullah Sk Senior Resident, Department of Nephrology, Institute of Post Graduate Medical Education & Research and SSKM Hospital, 244, A J C Bose Road, Kolkata-700020, India.
dc.description.abstractAbstract: Drug-induced alopecia, typically presenting as diffuse, non-scarring hair loss, is often reversible upon discontinuation of the offending medication. Cyclosporine A (CsA), an immunosuppressive agent frequently causing hypertrichosis, has been paradoxically reported to induce alopecia in rare cases. We report a 20-month-old girl with steroid-resistant nephrotic syndrome who developed severe alopecia due to a mistakenly taken high dose of cyclosporine. Upon discontinuation of cyclosporine, her hair began to regrow within a week. This case underscores the complexity of drug-induced alopecia and highlights the need for further research into the immune dysregulation associated with alopecia areata.
dc.identifierhttps://doi.org/10.60086/jnps1235
dc.identifier.urihttps://hdl.handle.net/20.500.14572/2679
dc.language.isoen_US
dc.publisherPerinatal Society of Nepal (PESON)
dc.subjectAlopecia areata
dc.subjectcyclosporine-induced alopecia
dc.subjectnephrotic syndrome
dc.titleCyclosporine-Induced Alopecia in Childhood Nephrotic Syndrome – A Case Report
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage61
oaire.citation.startPage59
relation.isJournalIssueOfPublication126c87f6-23d1-4cb3-aab2-6c44daaa6b53
relation.isJournalIssueOfPublication.latestForDiscovery126c87f6-23d1-4cb3-aab2-6c44daaa6b53
relation.isJournalOfPublication6f9be05c-05a9-4a3e-a5b5-a19a15ab042c

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