{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,14]],"date-time":"2026-02-14T01:04:32Z","timestamp":1771031072745,"version":"3.50.1"},"reference-count":12,"publisher":"Springer Publishing Company","issue":"6","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Neonatal Network"],"published-print":{"date-parts":[[2004,11]]},"abstract":"Epidermolysis bullosa (EB) is defined as a group of skin disorders that presents as blistering of the skin in varying degrees of severity. Most cases are inherited, but rare cases may be acquired. There are three main types: simplex, junctional, and dystrophic. The dermal-epidermal junction of the newborn skin is a vital area of attachment. Any defects in the components that comprise this junction can lead to fragility of the skin. EB diagnosis and testing can be performed both prenatally and postnatally. There is no cure for EB. Treatment revolves around supportive care and prevention of complications.The NICU nurse plays an important role on the multidisciplinary team as primary caregiver to the infant and educator to the family.<\/jats:p>","DOI":"10.1891\/0730-0832.23.6.25","type":"journal-article","created":{"date-parts":[[2011,11,16]],"date-time":"2011-11-16T09:35:20Z","timestamp":1321436120000},"page":"25-32","source":"Crossref","is-referenced-by-count":13,"title":["Epidermolysis Bullosa: Pathophysiology and Nursing Care"],"prefix":"10.1891","volume":"23","author":[{"given":"Barbara","family":"Gannon","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"793","published-online":{"date-parts":[[2004,11,1]]},"reference":[{"key":"1","unstructured":"Frieden IJ, and Howard R. 2001. Vesicles, pustules, bullae, erosions, and ulcerations. In Textbook of Neonatal Dermatology<\/i>, Eichenfield LF, Frieden IJ, and Esterly NB, eds. Philadelphia: WB Saunders, 158\u2013167."},{"key":"2","volume-title":"A Color Atlas of Life Before Birth: Normal Fetal Development.","author":"M. England","year":"1990"},{"issue":"1","key":"3","doi-asserted-by":"crossref","first-page":"63","DOI":"10.1097\/00005237-200006000-00006","article-title":"Neonatal skin disorders: A review of selected dermatologic abnormalities.","volume":"14","author":"JM Campbell","year":"2000","journal-title":"Journal of Perinatal and Neonatal Nursing"},{"issue":"2","key":"4","doi-asserted-by":"crossref","first-page":"190","DOI":"10.1001\/archderm.1986.01660140080023","article-title":"Severe infantile epidermolysis bullosa simplex: Dowling Meara subtype.","volume":"122","author":"L Buchbinder","year":"1986","journal-title":"Archives of Dermatology"},{"issue":"2","key":"5","doi-asserted-by":"crossref","first-page":"98","DOI":"10.1111\/j.1525-1470.1987.tb00760.x","article-title":"Acute laryngeal obstruction in junctional epidermolysis bullosa.","volume":"4","author":"H Davies","year":"1987","journal-title":"Pediatric Dermatology"},{"issue":"6","key":"6","doi-asserted-by":"crossref","first-page":"375","DOI":"10.1001\/archderm.1982.01650180009008","article-title":"Generalized atrophic benign epidermolysis bullosa.","volume":"118","author":"H Hintner","year":"1982","journal-title":"Archives of Dermatology"},{"issue":"5","key":"7","doi-asserted-by":"crossref","first-page":"617","DOI":"10.1111\/j.1365-2133.1994.tb13109.x","article-title":"Epidermolysis bullosa pruriginosa: Dystrophic epidermolysis bullosa with distinctive clinicopathological features.","volume":"130","author":"JA McGrath","year":"1994","journal-title":"British Journal of Dermatology"},{"key":"8","volume-title":"Epidermolysis Bullosa: Clinical, Epidermologic and Laboratory Advances and the Findings of the National Epidermolysis Bullosa Registry.","author":"JD Fine","year":"1999"},{"key":"9","doi-asserted-by":"crossref","unstructured":"Fine JD, et al. 2000. Revised classification system for inherited EB: Report of the Second International Consensus Meeting on Diagnosis and Classification of EB. Journal of the American Academy of Dermatology<\/i> 42(6): 1051\u20131066.","DOI":"10.1067\/mjd.2000.106369"},{"issue":"9","key":"10","doi-asserted-by":"crossref","first-page":"321","DOI":"10.1053\/siny.2000.0017","article-title":"Management of severe blistering disorders.","volume":"5","author":"J. Denyer","year":"2000","journal-title":"Seminars in Neonatology"},{"key":"11","unstructured":"Dystrophic Epidermolysis Bullosa Research Association of America (DebRA). 2003. General guidelines to the routine management and care of inherited epidermolysis bullosa, sections 1\u20135. Retrieved August 2004 from http:\/\/www.debra.org\/ index.php<\/a>"},{"key":"12","first-page":"124","article-title":"Epidermolysis Bullosa: Basic and Clinical Aspects.<\/i> New York: Springer","volume":"Verlag","author":"AN Lin","year":"1992","journal-title":"-"}],"container-title":["Neonatal Network"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1891\/0730-0832.23.6.25","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,9,18]],"date-time":"2019-09-18T17:25:32Z","timestamp":1568827532000},"score":1,"resource":{"primary":{"URL":"http:\/\/connect.springerpub.com\/lookup\/doi\/10.1891\/0730-0832.23.6.25"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2004,11]]},"references-count":12,"journal-issue":{"issue":"6","published-online":{"date-parts":[[2004,11,1]]},"published-print":{"date-parts":[[2004,11]]}},"alternative-id":["10.1891\/0730-0832.23.6.25"],"URL":"https:\/\/doi.org\/10.1891\/0730-0832.23.6.25","relation":{},"ISSN":["0730-0832","1539-2880"],"issn-type":[{"value":"0730-0832","type":"print"},{"value":"1539-2880","type":"electronic"}],"subject":[],"published":{"date-parts":[[2004,11]]}}}