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dc.contributor.CRUESPUNIVERSIDADE ESTADUAL DE CAMPINASpt_BR
dc.subject.otherCOGNITIVE DEFICITSen
dc.subject.otherRIDGE COUNTen
dc.subject.otherASYMMETRYen
dc.subject.otherDERMATOGLYPHICSen
dc.subject.otherADULTHOODen
dc.subject.otherBRAINen
dc.typeArtigo de periódicopt_BR
dc.type.categoryoriginal articlept_BR
dc.type.versionpublishedVersionpt_BR
dc.titlePsychogenetics of Turner syndrome: an investigation of 28 subjects and respective controls using the Bender test and Piagetian scalespt_BR
dc.contributor.authorRICARDI, F. C. F.pt_BR
dc.contributor.authorZAIA, L. L.pt_BR
dc.contributor.authorPELLEGRINO-ROSA, I.pt_BR
dc.contributor.authorROSA, J. T.pt_BR
dc.contributor.authorASSIS, O. Z. Mantovani dept_BR
dc.contributor.authorSALDANHA, P. H.pt_BR
unicamp.authorZAIA, L. L.:Universidade Estadual de Campinas, Faculdade de Educação, Laboratório de Psicologia Genéticapt_BR
unicamp.authorASSIS, O. Z. Mantovani de:Universidade Estadual de Campinas, Faculdade de Educação, Laboratório de Psicologia Genéticapt_BR
unicamp.author.externalPELLEGRINO-ROSA, I.pt
unicamp.author.externalRICARDI, F. C. F.pt
unicamp.author.externalROSA, J. T.pt
unicamp.author.externalSALDANHA, P. H.pt
dc.subjectTurner syndrome cognitionpt_BR
dc.subjectBender testpt_BR
dc.subjectPiagetian scalespt_BR
dc.subjectDermatoglyphicspt_BR
dc.subject.wosBiochemistry & Molecular Biologypt_BR
dc.subject.wosGenetics & Hereditypt_BR
dc.description.abstractPiagetian scales and the Bender visual motor gestalt test (BT) were applied to 28 subjects with universal 45, X Turner syndrome (TS), and their respective controls, in order to investigate their cognitive performance. Dermatoglyphics were also analyzed to obtain clues concerning embryological changes that may have appeared during development of the nervous system and could be associated with cognitive performance of TS patients. Dermatoglyphic pattern distribution was similar to that reported in previous studies of TS individuals: ulnar loops in the digital patterns and finger ridge, a-b, and A'-d counts were more frequent, while arch and whorl patterns were less frequent compared to controls. However, we did not find higher frequencies of hypothenar pattern, maximum atd angle, and ulnarity index in our TS subjects, unlike other investigations. Furthermore, we found significant differences between TS and control T line index values. The BT scores were also lower in probands, as has been previously reported, revealing a neurocognitive deficit of visual motor perception in TS individuals, which could be due to an absence of, or deficiency in, cerebral hemispheric lateralization. However, TS subjects seemed to improve their performance on BT with age. Cognitive performance of the TS subjects was not significantly different from that of controls, confirming a previous study in which TS performance was found to be similar to that of the normal Brazilian population. There were significant correlations between BT scores and Piagetian scale levels with dermatoglyphic parameters. This association could be explained by changes in the common ectodermal origin of the epidermis and the central nervous system. TS subjects seem to succeed in compensating their spatial impairments in adapting their cognitive and social contacts. We concluded that genetic counseling should consider cognitive and psychosocial difficulties presented by TS subjects, providing appropriate treatment and orientation for them and their families.en
dc.relation.ispartofGenetics and Molecular Researchpt_BR
dc.publisher.countryBrasilpt_BR
dc.publisherFUNPEC-EDITORApt_BR
dc.date.issued2010pt_BR
dc.identifier.citationGENETICS AND MOLECULAR RESEARCH, v.9, n.3, p.1701-1725, 2010pt_BR
dc.language.isoengpt_BR
dc.description.volume9pt_BR
dc.description.issuenumber3pt_BR
dc.description.firstpage1701pt_BR
dc.description.lastpage1725pt_BR
dc.rightsabertopt_BR
dc.rights.holderCopyright FUNPEC-EDITORApt_BR
dc.sourceWOSpt_BR
unicamp.cruespUSPpt_BR
dc.identifier.issn1676-5680pt_BR
dc.identifier.doi10.4238/vol9-3gmr815pt_BR
dc.identifier.urlhttp://dx.doi.org/10.4238/vol9-3gmr815pt_BR
dc.identifier.urlhttp://apps.isiknowledge.com/InboundService.do?Func=Frame&product=WOS&action=retrieve&SrcApp=EndNote&UT=000282756600028&Init=Yes&SrcAuth=ResearchSoft&mode=FullRecordpt_BR
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)pt_BR
dc.description.sponsorship1Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)pt_BR
dc.description.sponsorremissiveCNPq_Brasilpt_BR
dc.date.available2013-07-26T17:57:36Z
dc.date.available2016-06-28T19:51:20Z-
dc.date.accessioned2013-07-26T17:57:36Z
dc.date.accessioned2016-06-28T19:51:20Z-
dc.description.provenanceMade available in DSpace on 2013-07-26T17:57:36Z (GMT). No. of bitstreams: 2 art_RICARDI_Psychogenetics_of_Turner_syndrome_an_investigation_of_2010.pdf.txt: 83861 bytes, checksum: 179d85285766c54d3bb9b2ca416a8e88 (MD5) art_RICARDI_Psychogenetics_of_Turner_syndrome_an_investigation_of_2010.pdf: 590054 bytes, checksum: 6311eae4c8506c9f34f8372296db68c6 (MD5) Previous issue date: 2010en
dc.description.provenanceMade available in DSpace on 2016-06-28T19:51:20Z (GMT). No. of bitstreams: 2 art_RICARDI_Psychogenetics_of_Turner_syndrome_an_investigation_of_2010.pdf.txt: 83861 bytes, checksum: 179d85285766c54d3bb9b2ca416a8e88 (MD5) art_RICARDI_Psychogenetics_of_Turner_syndrome_an_investigation_of_2010.pdf: 590054 bytes, checksum: 6311eae4c8506c9f34f8372296db68c6 (MD5) Previous issue date: 2010en
dc.identifier.urihttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/331
dc.identifier.urihttp://repositorio.unicamp.br/jspui/handle/REPOSIP/331-
dc.contributor.departmentPsicologia
dc.contributor.unidadeFEpt
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