1. Identification and frequencies of cystic fibrosis mutations in central Argentina
- Author
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Teresinha Leal, Daniel Baran, Xavier Pepermans, Sergio Chialina, Vincent Bours, Hilda Lande, Walter Bordino, Soledad Mellado, Marta Wagener, and Liliana Gallardo
- Subjects
0301 basic medicine ,Heterozygote ,Cystic Fibrosis ,First line ,Clinical Biochemistry ,Population ,Argentina ,Bioinformatics ,Cystic fibrosis ,03 medical and health sciences ,symbols.namesake ,European origin ,medicine ,Humans ,Allele ,education ,Sanger sequencing ,Genetics ,education.field_of_study ,business.industry ,Homozygote ,General Medicine ,medicine.disease ,Phenotype ,030104 developmental biology ,Mutation ,symbols ,Identification (biology) ,business - Abstract
Background The Argentinian population is mainly of Caucasian origin, with a small contingent of indigenous descent. The aim of this study is to test the hypothesis that a panel of mutations designed for European countries is not optimal as a first-line molecular diagnosis for routine use in this country of mixed European origin. Methods Phenotype analyses combined with a European screening panel of 71 mutations followed by Sanger sequencing and large rearrangement study, were used to characterize the identification and distribution of CFTR mutations in the Santa Fe province of Argentina. Results Clinical review of 121 subjects suspected of CF during childhood led to selection of 83 unrelated patients. Thirty four different mutations, including two new ones, c.2554dupT and p.Leu49Pro, were detected. The total sensitivity was 91% (n = 151/166 alleles). Conclusions Frequencies of CFTR mutations in Argentinian populations differ from those of their European ancestry. A new first line panel of 21 CFTR mutations with a sensitivity of 84% is proposed for routine use in central Argentina.
- Published
- 2016
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