Article:
Dystrophic Epidermolysis Bullosa

creativeworkseries.issnJNMA Print ISSN: 0028-2715; Online ISSN: 1815-672X
dc.contributor.authorYadav, Randhir Sagar
dc.contributor.authorJayswal, Amar
dc.contributor.authorShrestha, Shumneva
dc.contributor.authorGupta, Sanjay Kumar
dc.contributor.authorPaudel, Upama
dc.date.accessioned2026-09-10T07:28:27Z
dc.date.available2026-09-10T07:28:27Z
dc.date.issued2018
dc.descriptionRandhir Sagar Yadav Maharajgunj Medical Campus, Institute of Medicine, Tribhuvan University, Kathmandu, Nepal https://orcid.org/0000-0003-4075-3544 Amar Jayswal Maharajgunj Medical Campus, Institute of Medicine, Tribhuvan University, Kathmandu, Nepal https://orcid.org/0000-0002-7365-9864 Shumneva Shrestha Maharajgunj Medical Campus, Institute of Medicine, Tribhuvan University, Kathmandu, Nepal https://orcid.org/0000-0001-7368-7884 Sanjay Kumar Gupta Department of General Practice and Emergency Medicine, Maharajgunj Medical Campus, Institute of Medicine, Tribhuvan University, Kathmandu, Nepal Upama Paudel Department of Dermatology, Maharajgunj Medical Campus, Institute of Medicine, Tribhuvan University, Kathmandu, Nepal
dc.description.abstractAbstract Epidermolysis bullosa is a rare inherited blistering disease with an incidence of 8-10 per million live births. Dystrophic epidermolysis bullosa is a type of epidermolysis bullosa caused by mutation in type VII collagen, COL7A1. There are 14 subtypes of dystrophic epidermolysis bullosa and 400 mutations of COL7A1. Electron microscopy is the gold standard diagnostic test but expensive. Immunofluorescence study is a suitable diagnostic alternative. Trauma prevention along with supportive care is the mainstay of therapy. Squamous cell carcinoma develops at an early age in epidermolysis bullosa than other patients, particularly in recessive dystrophic epidermolysis bullosa subtypes. Regular follow-up is imperative in detecting and preventing complications. Gene therapy, cell therapy and bone marrow transplantation are the emerging novel therapeutic innovations. Preventing possible skin and mucosal injury in patients requiring surgery should be worked on. Here, we present a case of dystrophic epidermolysis bullosa in a 26-year-old male.
dc.identifierhttps://doi.org/10.31729/jnma.3791
dc.identifier.urihttps://hdl.handle.net/20.500.14572/7618
dc.language.isoen_US
dc.publisherNepal Medical Association
dc.titleDystrophic Epidermolysis Bullosa
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage882
oaire.citation.startPage879
relation.isJournalIssueOfPublication6fca68af-9e2e-4701-9260-e69b19374e41
relation.isJournalIssueOfPublication.latestForDiscovery6fca68af-9e2e-4701-9260-e69b19374e41
relation.isJournalOfPublicatione6e146a0-0ece-4aba-aa0a-6ccfbd10a12a

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