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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/75222
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dc.contributor.authorMedeiros, G. X.-
dc.contributor.authorRiet-Correa, F.-
dc.contributor.authorBarros, S. S.-
dc.contributor.authorSoares, M. P.-
dc.contributor.authorDantas, A. F M-
dc.contributor.authorGaliza, G. J N-
dc.contributor.authorSimões, S. V D-
dc.contributor.authorBorges, Alexandre Secorun-
dc.date.accessioned2014-05-27T11:29:01Z-
dc.date.accessioned2016-10-25T18:47:56Z-
dc.date.available2014-05-27T11:29:01Z-
dc.date.available2016-10-25T18:47:56Z-
dc.date.issued2013-05-01-
dc.identifierhttp://dx.doi.org/10.1016/j.jcpa.2012.09.002-
dc.identifier.citationJournal of Comparative Pathology, v. 148, n. 4, p. 354-360, 2013.-
dc.identifier.issn0021-9975-
dc.identifier.issn1532-3129-
dc.identifier.urihttp://hdl.handle.net/11449/75222-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/75222-
dc.description.abstractClinical, histopathological and ultrastructural findings of caprine dystrophic epidermolysis bullosa (DEB) with autosomal recessive inheritance are reported. The goats presented with exungulation, erosions, crusts and scars on the skin and ulcers in the oral cavity. Microscopically, the skin showed subepidermal separation with clefts filled occasionally with clear eosinophilic fluid, cellular debris or neutrophils. Ultrastructurally, the site of blister formation was the sublamina densa in the epidermal basement membrane zone. In skin with blister formation and in clinically uninvolved skin, the basal lamina was preserved, but the anchoring fibrils were sparse and rudimentary. A twin brother of an affected kid was mated over 5 years with his mother; three out of the 10 kids born presented with epidermolysis bullosa, indicating that the disease has an autosomal recessive mode of inheritance. It is suggested that the disease is similar to human severe generalized recessive DEB. © 2012 Elsevier Ltd.en
dc.format.extent354-360-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectAnchoring fibrils-
dc.subjectBasal membrane-
dc.subjectEpidermolysis bullosa-
dc.subjectGoat-
dc.subjectanimal tissue-
dc.subjectautopsy-
dc.subjectautosomal recessive inheritance-
dc.subjectbasement membrane-
dc.subjectblister-
dc.subjectepidermolysis bullosa dystrophica-
dc.subjectgoat-
dc.subjecthair follicle-
dc.subjecthemidesmosome-
dc.subjecthistopathology-
dc.subjectkeratinocyte-
dc.subjectmalnutrition-
dc.subjectmouth ulcer-
dc.subjectneutrophil-
dc.subjectnonhuman-
dc.subjectpriority journal-
dc.subjectscar-
dc.subjectCapra-
dc.subjectCapra hircus-
dc.titleDystrophic Epidermolysis Bullosa in Goatsen
dc.typeoutro-
dc.contributor.institutionFederal University of Campina Grande-
dc.contributor.institutionFederal University of Pelotas-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationVeterinary Hospital Federal University of Campina Grande, Patos, Paraíba, CEP 58708-110-
dc.description.affiliationRegional Diagnostic Laboratory Veterinary Faculty Federal University of Pelotas, Pelotas, Rio Grande do Sul, CEP 96010-900-
dc.description.affiliationDepartment of Veterinary Clinical Science School of Veterinary Medicine and Animal Science São Paulo State University, UNESP, FMVD, Botucatu, SP 18618-000-
dc.description.affiliationUnespDepartment of Veterinary Clinical Science School of Veterinary Medicine and Animal Science São Paulo State University, UNESP, FMVD, Botucatu, SP 18618-000-
dc.identifier.doi10.1016/j.jcpa.2012.09.002-
dc.identifier.wosWOS:000319088300010-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of Comparative Pathology-
dc.identifier.scopus2-s2.0-84876784136-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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