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• W1869213667 abstract "Gaucher's disease ( GD ) is caused by a β‐glucocerebrosidase deficiency, leading to the accumulation of glucocerebroside in the reticuloendothelial system. The prevalence of GD in Tabuleiro do Norte ( TN ) (1:4000) is the highest in Brazil. The purpose of this study was to present evidence of consanguinity and founder effect for the G377S mutation (c. 1246G >A) among GD patients in TN based on enzyme, molecular and genealogical studies. Between March 2009 and December 2010, 131 subjects at risk for GD ( GC in dried blood ≤2.19 nmol/h/ml) and 5 confirmed GD patients from the same community were submitted for molecular analysis to characterize the genetic profile of the population. Based on the enzymatic and molecular analysis, the subjects were classified into three categories: affected ( n = 5), carrier ( n = 20) and non‐carrier ( n = 111). All carriers were ( G377S /wt). Affected subjects were homozygous ( G377S / G377S ). The identification of a single mutation in carriers and homozygotes from different generations, the history of the community and the genealogy study suggest that the high prevalence of GD in this population may be due to a combination of consanguinity and founder effect for the G377S mutation." @default.
• W1869213667 created "2016-06-24" @default.
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• W1869213667 date "2014-11-08" @default.
• W1869213667 modified "2023-10-14" @default.
• W1869213667 title "Consanguinity and founder effect for Gaucher disease mutation <scp>G377S</scp> in a population from Tabuleiro do Norte, Northeastern Brazil" @default.
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• W1869213667 doi "https://doi.org/10.1111/cge.12515" @default.
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