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dc.contributor.authorLobato, Maria Inês Rodriguespt_BR
dc.contributor.authorBelmonte-de-Abreu, Paulo Silvapt_BR
dc.contributor.authorKnijnik, Daniela Zippinpt_BR
dc.contributor.authorTeruchkin, Betinapt_BR
dc.contributor.authorGhisolfi, Eduardo Sorensenpt_BR
dc.contributor.authorHenriques, Alexandre Annespt_BR
dc.date.accessioned2010-04-24T04:15:29Zpt_BR
dc.date.issued2001pt_BR
dc.identifier.issn0100-879Xpt_BR
dc.identifier.urihttp://hdl.handle.net/10183/21145pt_BR
dc.description.abstractThe authors review environmental and neurodevelopmental risk factors for schizophrenic disorders, with emphasis on minor physical anomalies, particularly craniofacial anomalies and dermatoglyphic variations. The high prevalence of these anomalies among schizophrenic subjects supports the neurodevelopmental theory of the etiology of schizophrenia, since they suggest either genetically or epigenetically controlled faulty embryonic development of structures of ectodermal origin like brain and skin. This may disturb neurodevelopment that in turn may cause these subjects to be at increased risk for the development of schizophrenia and related disorders. The precise confirmation of this theory, at least in some cases, will provide further understanding of these illnesses, allowing easy and inexpensive identification of subjects at risk and providing guidelines for the development of new pharmacological interventions for early treatment and even for primary prevention of the illness.en
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofBrazilian journal of medical and biological research. Ribeirão Preto, SP. Vol. 34, no. 2 (Feb. 2001), p. 155-163pt_BR
dc.rightsOpen Accessen
dc.subjectSchizophreniaen
dc.subjectEsquizofreniapt_BR
dc.subjectNeurodevelopmental disorderen
dc.subjectFatores de riscopt_BR
dc.subjectRisk factorsen
dc.subjectCérebropt_BR
dc.subjectDeficiências do desenvolvimentopt_BR
dc.titleNeurodevelopmental risk factors in schizophreniapt_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb000284412pt_BR
dc.type.originNacionalpt_BR


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