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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/10739
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dc.contributor.authorLamonica, Dionisia A. C.-
dc.contributor.authorAbramides, Dagma Venturini Marques-
dc.contributor.authorMaximino, Luciana P.-
dc.contributor.authorGejao, Mariana G.-
dc.contributor.authorda Silva, Greyce K.-
dc.contributor.authorFerreira, Amanda T.-
dc.contributor.authorFurlan, Renata H.-
dc.contributor.authorGiacheti, Célia Maria-
dc.contributor.authorBarros-Neto, Plinio A.-
dc.contributor.authorRichieri-Costa, A.-
dc.date.accessioned2014-05-20T13:31:32Z-
dc.date.accessioned2016-10-25T16:50:10Z-
dc.date.available2014-05-20T13:31:32Z-
dc.date.available2016-10-25T16:50:10Z-
dc.date.issued2009-05-01-
dc.identifierhttp://dx.doi.org/10.1002/ajmg.a.32787-
dc.identifier.citationAmerican Journal of Medical Genetics Part A. Hoboken: Wiley-liss, v. 149A, n. 5, p. 1041-1045, 2009.-
dc.identifier.issn1552-4825-
dc.identifier.urihttp://hdl.handle.net/11449/10739-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/10739-
dc.description.abstractWe report oil the clinical, neuropsychological and language characteristics of it boy with left ventricular noncompaction cardiomyopathy (LVNC), agenesis of the splenium of the corpus callosum, minor anomalies of face and limbs, mild mental retardation, and speech and language disabilities. The occurrence of pilomatricoma (calcifying epithelioma) may be part of the clinical spectrum or a fortuitous finding. Compared to other related conditions with LVNC suggests that this is a new unique pattern MCA/MR syndrome. (C) 2009 Wiley-Liss, Inc.en
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)-
dc.format.extent1041-1045-
dc.language.isoeng-
dc.publisherWiley-liss-
dc.sourceWeb of Science-
dc.subjectleft ventricular noncompaction cardiomyopathyen
dc.subjectmental retardationen
dc.subjectspeech/language disordersen
dc.titlePossible New Syndrome: Left Ventricular Noncompaction, Partial Agenesis of the Corpus Callosum, and Developmental Delay in a Brazilian Childen
dc.typeoutro-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationHRAC USP, Dept Med Genet, BR-17012900 Bauru, SP, Brazil-
dc.description.affiliationFOB USP, Dept Fonoaudiol, Bauru, SP, Brazil-
dc.description.affiliationUNESP, Dept Fonoaudiol, Marilia, SP, Brazil-
dc.description.affiliationCentroCard Bauru, Bauru, SP, Brazil-
dc.description.affiliationUnespUNESP, Dept Fonoaudiol, Marilia, SP, Brazil-
dc.description.sponsorshipIdCNPq: 470996/2006-4-
dc.description.sponsorshipIdCNPq: 301926/2007-7-
dc.identifier.doi10.1002/ajmg.a.32787-
dc.identifier.wosWOS:000265805900035-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofAmerican Journal of Medical Genetics Part A-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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