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Provedor de dados:  Genet. Mol. Biol.
País:  Brazil
Título:  Inbreeding levels in Northeast Brazil: strategies for the prospecting of new genetic disorders
Autores:  Santos,Silvana
Kok,Fernando
Weller,Mathias
Paiva,Francisco Rennan Lopes de
Otto,Paulo A.
Data:  2010-01-01
Ano:  2010
Palavras-chave:  Inbreeding levels
Genetic drift
Geographic isolation
Resumo:  A new autosomal recessive genetic condition, the SPOAN syndrome (an acronym for spastic paraplegia, optic atrophy and neuropathy syndrome), was recently discovered in an isolated region of the State of Rio Grande do Norte in Northeast Brazil, in a population that was identified by the IBGE (Brazilian Institute of Geography and Statistics) as belonging to the Brazilian communities with the highest rates of "deficiencies" (Neri, 2003), a term used to describe diseases, malformations, and handicaps in general. This prompted us to conduct a study of consanguinity levels in five of its municipal districts by directly interviewing their inhabitants. Information on 7,639 couples (corresponding to about 40% of the whole population of the studied districts) was obtained. The research disclosed the existence of very high frequencies of consanguineous marriages, which varied from about 9% to 32%, suggesting the presence of a direct association between genetic diseases such as the SPOAN syndrome, genetic drift and inbreeding levels. This fact calls for the introduction of educational programs for the local populations, as well as for further studies aiming to identify and characterize other genetic conditions. Epidemiological strategies developed to collect inbreeding data, with the collaboration of health systems available in the region, might be very successful in the prospecting of genetic disorders.
Tipo:  Info:eu-repo/semantics/article
Idioma:  Inglês
Identificador:  http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572010000200003
Editor:  Sociedade Brasileira de Genética
Relação:  10.1590/S1415-47572010005000020
Formato:  text/html
Fonte:  Genetics and Molecular Biology v.33 n.2 2010
Direitos:  info:eu-repo/semantics/openAccess
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