Beckwith-Wiedemann syndrome and virilizing cortical adrenal tumor in a child

dc.creatorSbragia-Neto, L
dc.creatorMelo, AA
dc.creatorGuerra, G
dc.creatorMarini, SHVD
dc.creatorBaptista, MTM
dc.creatorde Matos, PS
dc.creatorde Oliveira, AG
dc.creatorBustorff-Silva, JM
dc.date2000
dc.dateAUG
dc.date2014-07-30T13:51:44Z
dc.date2015-11-26T16:41:06Z
dc.date2014-07-30T13:51:44Z
dc.date2015-11-26T16:41:06Z
dc.date.accessioned2018-03-28T23:25:12Z
dc.date.available2018-03-28T23:25:12Z
dc.identifierJournal Of Pediatric Surgery. W B Saunders Co, v. 35, n. 8, n. 1269, n. 1271, 2000.
dc.identifier0022-3468
dc.identifierWOS:000089146500028
dc.identifier10.1053/jpsu.2000.8771
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/55360
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/55360
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1272816
dc.descriptionThe authors report a case of a virilizing adrenal tumor that developed in a 2-year-old child with Beckwith-Wiedemann syndrome (BWS), He had a fetal diagnosis of omphalocele and a history of neonatal adrenal cysts. The importance of prenatal diagnosis of BWS and postnatal follow-up of tumors is discussed. The differential diagnosis of adrenal pathologies occurring in BWS also is reviewed. J Pediatr Surg 35:1269-1277. Copyright (C) 2000 by W.B. Saunders Company.
dc.description35
dc.description8
dc.description1269
dc.description1271
dc.languageen
dc.publisherW B Saunders Co
dc.publisherPhiladelphia
dc.publisherEUA
dc.relationJournal Of Pediatric Surgery
dc.relationJ. Pediatr. Surg.
dc.rightsfechado
dc.sourceWeb of Science
dc.subjectBeckwith-Wiedemann syndrome
dc.subjectadrenal gland diseases
dc.subjectadrenal
dc.subjectomphalocele
dc.subjectAdrenocortical Carcinoma
dc.subjectPrenatal-diagnosis
dc.subjectHemihypertrophy
dc.subjectNeoplasms
dc.titleBeckwith-Wiedemann syndrome and virilizing cortical adrenal tumor in a child
dc.typeArtículos de revistas


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