{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,6]],"date-time":"2026-09-06T21:47:52Z","timestamp":1788731272283,"version":"build-2803163510"},"reference-count":11,"publisher":"Oxford University Press (OUP)","issue":"11","license":[{"start":{"date-parts":[[2023,11,29]],"date-time":"2023-11-29T00:00:00Z","timestamp":1701216000000},"content-version":"vor","delay-in-days":28,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2023,11,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:p>Epidermolysis Bullosa is an inherited mechanobullous disorder which presents in the neonatal period as blistering skin lesions. In this case report, we describe an uncommon presentation of Epidermolysis Bullosa Simplex in a term infant, weighing 2640\u00a0g, born to a mother who was also diagnosed with Epidermolysis Bullosa Pruriginosa during the course of the evaluation of her newborn. The clinical situation presented us with a unique dilemma with regard to routine newborn care practices including handling, skin and diaper care. Though the presentation was typically characteristic of EB, we illustrate with images the diagnostic modalities and challenges faced in the hospital while caring for this fragile skin in a low and middle-income country\u2019s neonatal intensive care unit. This is the first reported case of a neonate with Epidermolysis Bullosa Simplex born to a mother with Epidermolysis Bullosa Pruriginosa.<\/jats:p>","DOI":"10.1093\/omcr\/omad124","type":"journal-article","created":{"date-parts":[[2023,11,29]],"date-time":"2023-11-29T13:51:58Z","timestamp":1701265918000},"source":"Crossref","is-referenced-by-count":1,"title":["Epidermolysis bullosa in a mother-infant dyad"],"prefix":"10.1093","volume":"2023","author":[{"given":"R R","family":"Prashanth","sequence":"first","affiliation":[{"name":"Seth G.S. Medical College and King Edward Memorial Hospital Department of Neonatology, , Maharashtra, Mumbai, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Pramod Dhanraj","family":"Kamble","sequence":"additional","affiliation":[{"name":"Seth G.S. Medical College and King Edward Memorial Hospital Department of Dermatology, , Maharashtra, Mumbai, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Abhilasha","family":"Kumari","sequence":"additional","affiliation":[{"name":"Seth G.S. Medical College and King Edward Memorial Hospital Department of Neonatology, , Maharashtra, Mumbai, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Anitha","family":"Haribalakrishna","sequence":"additional","affiliation":[{"name":"Seth G.S. Medical College and King Edward Memorial Hospital Department of Neonatology, , Maharashtra, Mumbai, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sunanda Arun","family":"Mahajan","sequence":"additional","affiliation":[{"name":"Seth G.S. Medical College and King Edward Memorial Hospital Department of Dermatology, , Maharashtra, Mumbai, India"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"286","published-online":{"date-parts":[[2023,11,28]]},"reference":[{"key":"2023112913514095500_ref1","doi-asserted-by":"crossref","first-page":"267","DOI":"10.4103\/ijpd.IJPD_16_17","article-title":"Inherited epidermolysis bullosa: a multisystem disease of skin and mucosae fragility","volume":"18","author":"Maldonado-Colin","year":"2017","journal-title":"Indian J Paediat Dermatol"},{"key":"2023112913514095500_ref2","doi-asserted-by":"crossref","first-page":"614","DOI":"10.1111\/bjd.18921","article-title":"Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility","volume":"183","author":"Has","year":"2020","journal-title":"Br J Dermatol"},{"key":"2023112913514095500_ref3","doi-asserted-by":"crossref","first-page":"e438","DOI":"10.1542\/neo.22-7-e438","article-title":"Diagnosis and Care of the Newborn with epidermolysis bullosa","volume":"22","author":"Lucky","year":"2021","journal-title":"NeoReviews"},{"key":"2023112913514095500_ref4","doi-asserted-by":"crossref","first-page":"387","DOI":"10.1097\/01.dad.0000211510.44865.6d","article-title":"A comparative study between transmission electron microscopy and immunofluorescence mapping in the diagnosis of epidermolysis bullosa","volume":"28","author":"Yiasemides","year":"2006","journal-title":"Am J Dermatopathol"},{"key":"2023112913514095500_ref5","doi-asserted-by":"crossref","first-page":"1215","DOI":"10.1111\/pde.14379","article-title":"Learning to pop blisters in epidermolysis bullosa with a simple model","volume":"37","author":"Sathishkumar","year":"2020","journal-title":"Pediatr Dermatol"},{"key":"2023112913514095500_ref6","doi-asserted-by":"crossref","first-page":"119","DOI":"10.1111\/pde.14444","article-title":"Characterization of wound microbes in epidermolysis bullosa: results from the epidermolysis bullosa clinical characterization and outcomes database","volume":"38","author":"Levin","year":"2021","journal-title":"Pediatr Dermatol"},{"key":"2023112913514095500_ref7","doi-asserted-by":"crossref","first-page":"721","DOI":"10.1016\/j.ijwd.2021.08.007","article-title":"Assessing the quality of life in the families of patients with epidermolysis bullosa: the mothers as main caregivers","volume":"7","author":"Chogani","year":"2021","journal-title":"Int J Womens Dermatol"},{"key":"2023112913514095500_ref8","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1186\/s13023-019-1279-y","article-title":"The challenges of living with and managing epidermolysis bullosa: insights from patients and caregivers","volume":"15","author":"Bruckner","year":"2020","journal-title":"Orphanet J Rare Dis"},{"key":"2023112913514095500_ref9","doi-asserted-by":"crossref","first-page":"S1","DOI":"10.1016\/j.ijwd.2017.02.002","article-title":"Retrospective evidence on outcomes and experiences of pregnancy and childbirth in epidermolysis bullosa in Australia and New Zealand","volume":"3","author":"Intong","year":"2017","journal-title":"Int J Womens Dermatol"},{"key":"2023112913514095500_ref10","first-page":"308","article-title":"Epidermolysis bullosa pruriginosa (McGrath) successfully controlled by oral cyclosporin","volume":"137","author":"Yamasaki","year":"1997","journal-title":"Br J Dermatol"},{"key":"2023112913514095500_ref11","doi-asserted-by":"crossref","first-page":"12","DOI":"10.1186\/1750-1172-5-12","article-title":"Inherited epidermolysis bullosa","volume":"5","author":"Fine","year":"2010","journal-title":"Orphanet J Rare Dis"}],"container-title":["Oxford Medical Case Reports"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/academic.oup.com\/omcr\/article-pdf\/2023\/11\/omad124\/53895680\/omad124.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"syndication"},{"URL":"https:\/\/academic.oup.com\/omcr\/article-pdf\/2023\/11\/omad124\/53895680\/omad124.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,11,29]],"date-time":"2023-11-29T13:52:06Z","timestamp":1701265926000},"score":1,"resource":{"primary":{"URL":"https:\/\/academic.oup.com\/omcr\/article\/doi\/10.1093\/omcr\/omad124\/7453336"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2023,11,1]]},"references-count":11,"journal-issue":{"issue":"11","published-print":{"date-parts":[[2023,11,1]]}},"URL":"https:\/\/doi.org\/10.1093\/omcr\/omad124","relation":{},"ISSN":["2053-8855"],"issn-type":[{"value":"2053-8855","type":"electronic"}],"subject":[],"published-other":{"date-parts":[[2023,11]]},"published":{"date-parts":[[2023,11,1]]},"article-number":"omad124"}}