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System medicine approach to improve diagnosis and prognosis in Autism Spectrum Disorder (ASD), based on extensive genomic, biochemical and clinical data

dc.contributor.authorAsif, Muhammad
dc.contributor.authorVicente, A.M.
dc.contributor.authorCouto, Francisco M.
dc.date.accessioned2016-02-16T13:34:10Z
dc.date.available2016-02-16T13:34:10Z
dc.date.issued2015-01-16
dc.description.abstractBackground: Autism Spectrum Disorder (ASD) is characterized by social communication impairments and repetitive behaviors, a clinical presentation spectrum and a high male to female ratio. Twin and family studies indicated a strong genetic basis for ASD, with approximately 20% of ASD etiologies residing with identified genetic abnormalities. Behavioral traits in the ASD spectrum are prevalent in unaffected family members, highlighting a trait heritability likely mediated by genetic factors that impact ASD risk. However, the impact of genetic factors on the phenotype and its variability is still not well understood. Due to the absence of underlying biological markers, ASD is still diagnosed by assessing the individual’s behavior. The understanding of the biological basis of ASD can contribute to an earlier diagnosis and then to early intervention, which can have a substantial positive effect on child developmen.pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.18/3325
dc.language.isoengpt_PT
dc.publisherInstituto Nacional de Saúde Doutor Ricardo Jorge, IPpt_PT
dc.subjectPerturbações do Desenvolvimento Infantil e Saúde Mentalpt_PT
dc.subjectAutismopt_PT
dc.subjectAutism Spectrum Disorderpt_PT
dc.titleSystem medicine approach to improve diagnosis and prognosis in Autism Spectrum Disorder (ASD), based on extensive genomic, biochemical and clinical datapt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceLisboa, Portugalpt_PT
oaire.citation.title1st BioSys PhD Day, Salão Nobre – Rectory of the University of Lisboa, 16th January 2015pt_PT
rcaap.rightsembargoedAccesspt_PT
rcaap.typeconferenceObjectpt_PT

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