Literature DB >> 7923859

Gaucher disease: N370S glucocerebrosidase gene frequency in the Portuguese population.

L Lacerda1, O Amaral, R Pinto, P Oliveira, J Aerts, M C Sá Miranda.   

Abstract

In the Portuguese population the most frequent form of Gaucher disease is type 1. The N370S glucocerebrosidase gene mutation accounts for 63% of mutated alleles. The frequency of this mutation was accurately determined in the Portuguese population, which does not present an Ashkenazi Jewish genetic background. A gene frequency of 0.0043, with 95% confidence limits between 0.0023 and 0.0063, was obtained studying the genomic DNA of 2000 blood cards randomly sampled from the national neonatal screening program. On the basis of this frequency a significantly high number of homozygotes for the N370S mutation should be expected in the Portuguese population. This finding supports the idea that the majority of homozygotes for this mutation present a very mild clinical phenotype and remain undiagnosed.

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Year:  1994        PMID: 7923859     DOI: 10.1111/j.1399-0004.1994.tb04034.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  6 in total

1.  Geographic distribution of disease mutations in the Ashkenazi Jewish population supports genetic drift over selection.

Authors:  Neil Risch; Hua Tang; Howard Katzenstein; Josef Ekstein
Journal:  Am J Hum Genet       Date:  2003-02-24       Impact factor: 11.025

2.  Gaucher disease: the origins of the Ashkenazi Jewish N370S and 84GG acid beta-glucosidase mutations.

Authors:  G A Diaz; B D Gelb; N Risch; T G Nygaard; A Frisch; I J Cohen; C S Miranda; O Amaral; I Maire; L Poenaru; C Caillaud; M Weizberg; P Mistry; R J Desnick
Journal:  Am J Hum Genet       Date:  2000-04-21       Impact factor: 11.025

3.  Complete screening for glucocerebrosidase mutations in Parkinson disease patients from Portugal.

Authors:  Jose Bras; Coro Paisan-Ruiz; Rita Guerreiro; Maria Helena Ribeiro; Ana Morgadinho; Cristina Januario; Ellen Sidransky; Catarina Oliveira; Andrew Singleton
Journal:  Neurobiol Aging       Date:  2007-12-21       Impact factor: 4.673

4.  Mapping the genetic and clinical characteristics of Gaucher disease in the Iberian Peninsula.

Authors:  Pilar Giraldo; Pilar Alfonso; Pilar Irún; Laura Gort; Amparo Chabás; Lluïsa Vilageliu; Daniel Grinberg; Clara M Sá Miranda; Miguel Pocovi
Journal:  Orphanet J Rare Dis       Date:  2012-03-19       Impact factor: 4.123

5.  Homozygous N396T mutation in Gaucher disease: Portuguese sisters with markedly different phenotypes.

Authors:  Samantha Kimball; Francis Choy; Agnes Zay; Dominick Amato
Journal:  Int Med Case Rep J       Date:  2011-03-16

6.  Gaucher disease: Biochemical and molecular findings in 141 patients diagnosed in Greece.

Authors:  Evangelia Dimitriou; Marina Moraitou; Mónica Cozar; Jenny Serra-Vinardell; Lluïsa Vilageliu; Daniel Grinberg; Irene Mavridou; Helen Michelakakis
Journal:  Mol Genet Metab Rep       Date:  2020-06-07
  6 in total

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