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dc.contributor.authorCastilla, Eduardo Enriquept_BR
dc.contributor.authorFaccini, Lavinia Schulerpt_BR
dc.date.accessioned2015-11-07T02:36:42Zpt_BR
dc.date.issued2014pt_BR
dc.identifier.issn1415-4757pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/128988pt_BR
dc.description.abstractHere we propose a registration process for population genetic isolates, usually geographic clusters of genetic disorders, based on the systematic search of rumors, defined as any type of account regardless of its reliability. Systematically ascertained rumors are recorded, and validated through a progressive process of pre-established steps. This paper outlines the conceptual basis for this approach and presents the preliminary results from a rumor-based nationwide registry of genetically isolated populations, named CENISO (Censo Nacional de Isolados), operating in Brazil since 2009. During the first four years of its existence (2009-2013), a total of 191 Rumors were registered and validated, resulting in a prevalence rate of one per million inhabitants of Brazil. When the five statutory geographic regions of Brazil were considered, more Rumors were registered for the Northeast (2.11; 1.74-2.54 per 106) than for the remaining four regions, North, Center-West, Southeast, and South, which did not differ among themselves. About half (86/191) of the recorded rumors were proven to be geographic clusters; of these disorders, 58 were autosomal recessive, 17 autosomal dominant, 5 X-linked, 3 multifactorial, and one environmental (thalidomide embryopathy).en
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofGenetics and molecular biology. Ribeirão Preto, SP. Vol. 37, n. 1 supl. (Apr. 2014), p. 186-193pt_BR
dc.rightsOpen Accessen
dc.subjectRumorsen
dc.subjectDoenças genéticaspt_BR
dc.subjectPopulaçãopt_BR
dc.subjectDisease clusteringen
dc.subjectGenetic diseasesen
dc.subjectPopulation registersen
dc.subjectBrazilen
dc.titleFrom rumors to genetic isolatespt_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb000917802pt_BR
dc.type.originNacionalpt_BR


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