Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/26309
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dc.contributor.authorBertola, D. R.
dc.contributor.authorKim, C. A.
dc.contributor.authorSugayama, SMM
dc.contributor.authorAlbano, LMJ
dc.contributor.authorUtagawa, C. Y.
dc.contributor.authorGonzalez, C. H.
dc.date.accessioned2016-01-24T12:31:05Z-
dc.date.available2016-01-24T12:31:05Z-
dc.date.issued2000-05-01
dc.identifierhttp://dx.doi.org/10.1046/j.1525-1470.2000.01756.x
dc.identifier.citationPediatric Dermatology. Malden: Blackwell Science Inc, v. 17, n. 3, p. 218-221, 2000.
dc.identifier.issn0736-8046
dc.identifier.urihttp://repositorio.unifesp.br/handle/11600/26309-
dc.description.abstractAmong the ectodermal dysplasias, there are several examples of overlapping phenotypes in disorders that are considered distinct. We report a 5-year-old boy born to nonconsanguineous parents and presenting with ectodermal dysplasia, ankyloblepharon filiforme adnatum, and bilateral choanal atresia consistent with the diagnosis of AEC syndrome. We compare the findings in our patient with the previous reported cases and discuss the overlapping phenotype of this disorder with CHAND syndrome.en
dc.format.extent218-221
dc.language.isoeng
dc.publisherBlackwell Science Inc
dc.relation.ispartofPediatric Dermatology
dc.rightsAcesso restrito
dc.titleAEC syndrome and CHAND syndrome: Further evidence of clinical overlapping in the ectodermal dysplasiasen
dc.typeArtigo
dc.contributor.institutionUniversidade Federal de São Paulo (UNIFESP)
dc.description.affiliationUniv São Paulo, FM, Hosp Clin, Inst Crianca,Dept Pediat, BR-05403900 São Paulo, Brazil
dc.identifier.doi10.1046/j.1525-1470.2000.01756.x
dc.description.sourceWeb of Science
dc.identifier.wosWOS:000087863800012
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