{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,14]],"date-time":"2026-10-14T01:22:51Z","timestamp":1791940971651,"version":"4.3.4"},"reference-count":40,"publisher":"Elsevier BV","issue":"3","license":[{"start":{"date-parts":[[2024,5,1]],"date-time":"2024-05-01T00:00:00Z","timestamp":1714521600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2024,5,1]],"date-time":"2024-05-01T00:00:00Z","timestamp":1714521600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2024,2,2]],"date-time":"2024-02-02T00:00:00Z","timestamp":1706832000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Anais Brasileiros de Dermatologia"],"published-print":{"date-parts":[[2024,5]]},"DOI":"10.1016\/j.abd.2023.06.009","type":"journal-article","created":{"date-parts":[[2024,2,24]],"date-time":"2024-02-24T13:06:59Z","timestamp":1708780019000},"page":"380-390","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":10,"title":["Hereditary epidermolysis bullosa: clinical-epidemiological profile of 278 patients at a tertiary hospital in S\u00e3o Paulo, Brazil"],"prefix":"10.1016","volume":"99","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-3188-959X","authenticated-orcid":false,"given":"Chan I.","family":"Thien","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-8713-3129","authenticated-orcid":false,"given":"Vanessa Rolim","family":"Bessa","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-8622-3800","authenticated-orcid":false,"given":"Isadora Zago","family":"Miotto","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-7077-8553","authenticated-orcid":false,"given":"Luciana Paula","family":"Samorano","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-2910-7330","authenticated-orcid":false,"given":"Maria Cec\u00edlia","family":"Rivitti-Machado","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-8596-1999","authenticated-orcid":false,"given":"Zilda Najjar Prado de","family":"Oliveira","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.abd.2023.06.009_bib0005","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":"10.1016\/j.abd.2023.06.009_bib0010","doi-asserted-by":"crossref","first-page":"78","DOI":"10.1038\/s41572-020-0210-0","article-title":"Epidermolysis bullosa","volume":"6","author":"Bardhan","year":"2020","journal-title":"Nat Rev Dis Primers"},{"key":"10.1016\/j.abd.2023.06.009_bib0015","doi-asserted-by":"crossref","first-page":"189","DOI":"10.1111\/cge.13555","article-title":"An overview of the genetic basis of epidermolysis bullosa in Brazil: discovery of novel and recurrent disease-causing variants","volume":"96","author":"Mariath","year":"2019","journal-title":"Clin Genet"},{"key":"10.1016\/j.abd.2023.06.009_bib0020","doi-asserted-by":"crossref","first-page":"551","DOI":"10.1016\/j.abd.2020.05.001","article-title":"Inherited epidermolysis bullosa: update on the clinical and genetic aspects","volume":"95","author":"Mariath","year":"2020","journal-title":"An Bras Dermatol"},{"key":"10.1016\/j.abd.2023.06.009_bib0025","doi-asserted-by":"crossref","first-page":"743","DOI":"10.1590\/S0365-05962011000400017","article-title":"Epidermolysis bullosa nevi: clinical, dermatoscopical and histological features in a case of recessive dystrofic form","volume":"86","author":"Melo","year":"2011","journal-title":"An Bras Dermatol"},{"key":"10.1016\/j.abd.2023.06.009_bib0030","first-page":"1035","article-title":"Underrecognition of epidermolysis bullosa pruriginosa","volume":"13","author":"Cha","year":"2015","journal-title":"J Dtsch Dermatol Ges"},{"key":"10.1016\/j.abd.2023.06.009_bib0035","doi-asserted-by":"crossref","DOI":"10.1111\/ddg.12258","article-title":"Clinical, dermoscopic and histopathological features of melanocytic nevi in dystrophic epidermolysis bullosa","volume":"12","author":"Fernandes","year":"2014","journal-title":"J Dtsch Dermatol Ges"},{"key":"10.1016\/j.abd.2023.06.009_bib0040","doi-asserted-by":"crossref","first-page":"155","DOI":"10.1016\/j.abd.2020.05.015","article-title":"Gene panel for the diagnosis of epidermolysis bullosa: proposal for a viable and efficient approach","volume":"96","author":"Mariath","year":"2021","journal-title":"An Bras Dermatol"},{"key":"10.1016\/j.abd.2023.06.009_bib0045","doi-asserted-by":"crossref","first-page":"126","DOI":"10.1590\/abd1806-4841.20175952","article-title":"Pretibial dystrophic epidermolysis bullosa","volume":"92","author":"Callegaro","year":"2017","journal-title":"An Bras Dermatol"},{"key":"10.1016\/j.abd.2023.06.009_bib0050","doi-asserted-by":"crossref","first-page":"856","DOI":"10.1590\/S0365-05962010000600012","article-title":"Immunological mapping in hereditary epidermolysis bullosa","volume":"85","author":"Oliveira","year":"2010","journal-title":"An Bras Dermatol"},{"key":"10.1016\/j.abd.2023.06.009_bib0055","doi-asserted-by":"crossref","first-page":"29","DOI":"10.1111\/cge.13792","article-title":"Genotype-phenotype correlations on epidermolysis bullosa with congenital absence of skin: a comprehensive review","volume":"99","author":"Mariath","year":"2021","journal-title":"Clin Genet"},{"key":"10.1016\/j.abd.2023.06.009_bib0060","doi-asserted-by":"crossref","first-page":"1126","DOI":"10.1111\/ijd.15634","article-title":"Prevalence and antimicrobial resistance profile of Staphylococcus aureus in inherited epidermolysis bullosa: a cross-sectional multicenter study in Brazil","volume":"60","author":"Santin","year":"2021","journal-title":"Int J Dermatol"},{"key":"10.1016\/j.abd.2023.06.009_bib0065","doi-asserted-by":"crossref","first-page":"536","DOI":"10.1016\/j.abd.2019.08.033","article-title":"Sporadic form of epidermolysis bullosa simplex with mottled pigmentation","volume":"95","author":"Ferreira","year":"2020","journal-title":"An Bras Dermatol"},{"key":"10.1016\/j.abd.2023.06.009_bib0070","doi-asserted-by":"crossref","first-page":"149","DOI":"10.1007\/978-3-319-67144-4_8","article-title":"Data quality in rare diseases registries","volume":"1031","author":"Kodra","year":"2017","journal-title":"Adv Exp Med Biol"},{"key":"10.1016\/j.abd.2023.06.009_bib0075","doi-asserted-by":"crossref","first-page":"765","DOI":"10.1111\/bjd.21295","article-title":"The importance of accurate epidemiological data of epidermolysis bullosa","volume":"186","author":"Baardman","year":"2022","journal-title":"Br J Dermatol"},{"key":"10.1016\/j.abd.2023.06.009_bib0080","doi-asserted-by":"crossref","first-page":"2211","DOI":"10.1056\/NEJMoa2206663","article-title":"Trial of beremagene geperpavec (B-VEC) for dystrophic epidermolysis bullosa","volume":"387","author":"Guide","year":"2022","journal-title":"N Engl J Med"},{"key":"10.1016\/j.abd.2023.06.009_bib0085","doi-asserted-by":"crossref","first-page":"99","DOI":"10.52547\/wjps.10.3.99","article-title":"Epidermolysis bullosa registry data in Iran","volume":"10","author":"Farokhforghani","year":"2021","journal-title":"World J Plast Surg"},{"key":"10.1016\/j.abd.2023.06.009_bib0090","doi-asserted-by":"crossref","first-page":"169","DOI":"10.1111\/pde.12258","article-title":"A survey of epidermolysis bullosa care in the United States and Canada","volume":"31","author":"Ahmad","year":"2014","journal-title":"Pediatr Dermatol"},{"key":"10.1016\/j.abd.2023.06.009_bib0095","doi-asserted-by":"crossref","first-page":"635","DOI":"10.1001\/archdermatol.2010.109","article-title":"Epidemiology of epidermolysis bullosa in the antipodes: the Australasian epidermolysis bullosa registry with a focus on Herlitz junctional epidermolysis bullosa","volume":"146","author":"Kho","year":"2010","journal-title":"Arch Dermatol"},{"key":"10.1016\/j.abd.2023.06.009_bib0100","doi-asserted-by":"crossref","first-page":"995","DOI":"10.1111\/jdv.17012","article-title":"Novel insights into the epidemiology of epidermolysis bullosa (EB) from the Dutch EB registry: EB more common than previously assumed?","volume":"35","author":"Baardman","year":"2021","journal-title":"J Eur Acad Dermatol Venereol"},{"key":"10.1016\/j.abd.2023.06.009_bib0105","doi-asserted-by":"crossref","first-page":"402","DOI":"10.1111\/jdv.18637","article-title":"Epidemiology of inherited epidermolysis bullosa in Germany","volume":"37","author":"Has","year":"2023","journal-title":"J Eur Acad Dermatol Venereol"},{"key":"10.1016\/j.abd.2023.06.009_bib0110","doi-asserted-by":"crossref","first-page":"873","DOI":"10.2340\/00015555-2929","article-title":"Genotype-Phenotype correlations of dystrophic epidermolysis bullosa in India: experience from a Tertiary Care Centre","volume":"98","author":"Yenamandra","year":"2018","journal-title":"Acta Derm Venereol"},{"key":"10.1016\/j.abd.2023.06.009_bib0115","doi-asserted-by":"crossref","first-page":"899","DOI":"10.1111\/jdv.12709","article-title":"Epidemiology of inherited epidermolysis bullosa in Romania and genotype-phenotype correlations in patients with dystrophic epidermolysis bullosa","volume":"29","author":"D\u0103nescu","year":"2015","journal-title":"J Eur Acad Dermatol Venereol"},{"key":"10.1016\/j.abd.2023.06.009_bib0120","doi-asserted-by":"crossref","DOI":"10.3389\/fgene.2021.753229","article-title":"Genetic profile of epidermolysis bullosa cases in King Abdulaziz Medical City, Riyadh, Saudi Arabia","volume":"12","author":"Alharthi","year":"2022","journal-title":"Front Genet"},{"key":"10.1016\/j.abd.2023.06.009_bib0125","doi-asserted-by":"crossref","first-page":"387","DOI":"10.1016\/j.jaad.2009.03.053","article-title":"Extracutaneous manifestations and complications of inherited epidermolysis bullosa: part II. Other organs","volume":"61","author":"Fine","year":"2009","journal-title":"J Am Acad Dermatol"},{"key":"10.1016\/j.abd.2023.06.009_bib0130","first-page":"160","article-title":"Hand care in epidermolysis bullosa","volume":"21","author":"Lima","year":"2011","journal-title":"Eur J Pediat Dermatol"},{"key":"10.1016\/j.abd.2023.06.009_bib0135","doi-asserted-by":"crossref","first-page":"33","DOI":"10.1080\/2000656X.2019.1661846","article-title":"Surgical management of hand deformities in patients with recessive dystrophic epidermolysis bullosa","volume":"54","author":"Zhou","year":"2020","journal-title":"J Plast Surg Hand Surg"},{"key":"10.1016\/j.abd.2023.06.009_bib0140","doi-asserted-by":"crossref","first-page":"147","DOI":"10.1097\/MPG.0b013e31812f5667","article-title":"Gastrointestinal complications of inherited epidermolysis bullosa: cumulative experience of the national epidermolysis bullosa registry","volume":"46","author":"Fine","year":"2008","journal-title":"J Pediatr Gastroenterol Nutr"},{"key":"10.1016\/j.abd.2023.06.009_bib0145","doi-asserted-by":"crossref","first-page":"203","DOI":"10.1016\/j.jaad.2008.09.035","article-title":"Epidermolysis bullosa and the risk of life-threatening cancers: the National EB registry experience, 1986-2006","volume":"60","author":"Fine","year":"2009","journal-title":"J Am Acad Dermatol"},{"key":"10.1016\/j.abd.2023.06.009_bib0150","first-page":"87","article-title":"Epiderm\u00f3lise bolhosa distr\u00f3fica e juncional: aspectos gastrointestinais","volume":"27","author":"Barbosa","year":"2005","journal-title":"Pediatria (S\u00e3o Paulo)"},{"key":"10.1016\/j.abd.2023.06.009_bib0155","doi-asserted-by":"crossref","first-page":"1195","DOI":"10.1001\/jamadermatol.2013.4833","article-title":"Malignant melanoma arising in the setting of epidermolysis bullosa simplex: an important distinction from epidermolysis bullosa nevus","volume":"149","author":"Hocker","year":"2013","journal-title":"JAMA Dermatol"},{"key":"10.1016\/j.abd.2023.06.009_bib0160","doi-asserted-by":"crossref","first-page":"1148","DOI":"10.1001\/jamadermatol.2013.5628","article-title":"Malignant melanoma and epidermolysis bullosa simplex","volume":"149","author":"Fine","year":"2013","journal-title":"JAMA Dermatol"},{"key":"10.1016\/j.abd.2023.06.009_bib0165","doi-asserted-by":"crossref","first-page":"97","DOI":"10.1111\/j.1365-2133.2005.06579.x","article-title":"Epidermolysis bullosa naevi reveal a distinctive dermoscopic pattern","volume":"153","author":"Lanschuetzer","year":"2005","journal-title":"Br J Dermatol"},{"key":"10.1016\/j.abd.2023.06.009_bib0170","doi-asserted-by":"crossref","first-page":"438","DOI":"10.2340\/00015555-0484","volume":"88","author":"Dang","year":"2008","journal-title":"Acta Derm Venereol"},{"key":"10.1016\/j.abd.2023.06.009_bib0175","doi-asserted-by":"crossref","first-page":"931","DOI":"10.1001\/archderm.1989.01670190065007","article-title":"Autosomal recessive epidermolysis bullosa simplex. Generalized phenotypic features suggestive of junctional or dystrophic epidermolysis bullosa, and association with neuromuscular diseases","volume":"125","author":"Fine","year":"1989","journal-title":"Arch Dermatol"},{"key":"10.1016\/j.abd.2023.06.009_bib0180","first-page":"677","article-title":"The risk of cardiomyopathy in inherited epidermolysis bullosa","volume":"159","author":"Fine","year":"2008","journal-title":"Br J Dermatol"},{"key":"10.1016\/j.abd.2023.06.009_bib0185","doi-asserted-by":"crossref","first-page":"360","DOI":"10.4103\/ijd.IJD_131_20","article-title":"Utility of immunofluorescence antigen mapping in hereditary epidermolysis bullosa","volume":"66","author":"Rao","year":"2021","journal-title":"Indian J Dermatol"},{"key":"10.1016\/j.abd.2023.06.009_bib0190","doi-asserted-by":"crossref","first-page":"94","DOI":"10.1111\/bjd.13190","article-title":"Whole-exome sequencing improves mutation detection in a diagnostic epidermolysis bullosa laboratory","volume":"172","author":"Takeichi","year":"2015","journal-title":"Br J Dermatol"},{"key":"10.1016\/j.abd.2023.06.009_bib0195","doi-asserted-by":"crossref","first-page":"70","DOI":"10.2340\/00015555-2781","article-title":"Epidemiology and Outcome of Squamous Cell Carcinoma in Epidermolysis Bullosa in Australia and New Zealand","volume":"98","author":"Kim","year":"2018","journal-title":"Acta Derm Venereol"},{"key":"10.1016\/j.abd.2023.06.009_bib0200","doi-asserted-by":"crossref","first-page":"391","DOI":"10.1016\/j.det.2010.02.013","article-title":"Epidermolysis bullosa care in Canada","volume":"28","author":"Pope","year":"2010","journal-title":"Dermatol Clin"}],"container-title":["Anais Brasileiros de Dermatologia"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0365059624000199?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0365059624000199?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,5,19]],"date-time":"2025-05-19T15:00:51Z","timestamp":1747666851000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0365059624000199"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2024,5]]},"references-count":40,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2024,5]]}},"alternative-id":["S0365059624000199"],"URL":"https:\/\/doi.org\/10.1016\/j.abd.2023.06.009","relation":{},"ISSN":["0365-0596"],"issn-type":[{"value":"0365-0596","type":"print"}],"subject":[],"published":{"date-parts":[[2024,5]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Hereditary epidermolysis bullosa: clinical-epidemiological profile of 278 patients at a tertiary hospital in S\u00e3o Paulo, Brazil","name":"articletitle","label":"Article Title"},{"value":"Anais Brasileiros de Dermatologia","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.abd.2023.06.009","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2024 Sociedade Brasileira de Dermatologia. Published by Elsevier Espa\u00f1a, S.L.U.","name":"copyright","label":"Copyright"}]}}