Literature DB >> 23670391

[Could endogamy explain the higher prevalence of disabilities in the population of the Brazilian Northeast?].

Silvana Cristina dos Santos1, Uirá Souto Melo, Simone Silva dos Santos Lopes, Mathias Weller, Fernando Kok.   

Abstract

Despite conceptual inaccuracies and methods of measurement, the WHO estimates that about 10% of the world population has some form of disability. In order to investigate the prevalence and etiology of disabilities and to evaluate if they could be associated with inbreeding, a cross-sectional epidemiological study was conducted using the informant method in five communities of the state Rio Grande do Norte in the Brazilian Northeast, in which consanguineous marriages frequencies varied between 9 and 32%. The average prevalence of disabilities in the five sampled communities was 4.53%, obtained by interviews that involved 37.87% of a population of 39,054 inhabitants. On average, 25% of consanguineous and 12% of non-consanguineous couples had one or more children with disabilities. The increased rate of individuals with disabilities in the Brazilian Northeast could be associated with the maintenance of the tradition of consanguineous marriages in these populations and some of these disabilities may be caused by genetic disorders.

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Mesh:

Year:  2013        PMID: 23670391     DOI: 10.1590/s1413-81232013000400027

Source DB:  PubMed          Journal:  Cien Saude Colet        ISSN: 1413-8123


  5 in total

1.  Increased prevalence of inherited neuromuscular disorders due to endogamy in Northeast Brazil: the need of community genetics services.

Authors:  Silvana Santos; Anne Aluska da Silva Pequeno; André Pessoa; Claudia Regina Cabral Galvão; Jovany Luiz Alves de Medeiros; Weller Mathias; Fernando Kok
Journal:  J Community Genet       Date:  2013-11-26

2.  Analyzing Inbreeding and Estimating Its Related Deficiencies in Northeastern Brazil.

Authors:  Cristian Rodrigues do Nascimento; Dyowani Dos Santos Basílio; Johnnatas Mikael Lopes; Isaac Farias Cansanção
Journal:  J Pediatr Genet       Date:  2021-04-01

3.  A large family with CYLD cutaneous syndrome: medical genetics at the community level.

Authors:  Anderson Pontes Arruda; Augusto César Cardoso-Dos-Santos; Luiza Monteavaro Mariath; Mariléa Furtado Feira; Thayne Woycinck Kowalski; Kalina Ribeiro Fontenele Bezerra; Leonardo Augusto Coelho Torres da Silva; Erlane Marques Ribeiro; Lavinia Schuler-Faccini
Journal:  J Community Genet       Date:  2019-12-03

4.  Inclusion and exclusion in the globalisation of genomics; the case of rare genetic disease in Brazil.

Authors:  Sahra Gibbon; Waleska Aureliano
Journal:  Anthropol Med       Date:  2018-04

5.  IDENTIFICATION OF MUTATIONS IN THE PAH GENE IN PKU PATIENTS IN THE STATE OF MATO GROSSO.

Authors:  Roseli Divino Costa; Bianca Borsatto Galera; Bianca Costa Rezende; Amanda Cristina Venâncio; Marcial Francis Galera
Journal:  Rev Paul Pediatr       Date:  2020-02-14
  5 in total

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