Molecular genetic study of cystic fibrosis in the Chilean population. Relationship to its clinical expression
Aspillaga, M.; Avendaño, I.; Largo, I.; Valenzuela, C.; Riveros, N.; Orellana, O.; Moreno, M.A.
Revista Medica de Chile 121(11): 1233-1239
1993
ISSN/ISBN: 0034-9887 PMID: 8191128 Document Number: 408251
Aiming to establish a genotype-phenotype relationship and to search a clinical expression in heterozygotes, 25 Chilean subjects with Cystic Fibrosis and 165 relatives were subjected to a clinical-molecular study. The most common mutations found worldwide were studied: delta F-508, G-542X, N-1303K, R-553X and G551D. Clinical and laboratory assessment comprised chest X-rays, spirometry, clinical evaluation, nutritional assessment, sweat test and carotenemia. Age at diagnosis was lower among homozygotes for the mutation delta F-508. In this group, Brasfield and Schawchman scores were better, probably due to an earlier initiation of treatment. No other differences were found among genotypic groups or relatives. Genetic markers indicated a higher european component of the sample, compared to the general Chilean population.