Estudio clínico-genético molecular de la fibrosis quística en la V Región, Chile

• Graciela Molina F ^[1] ; Francisco J González R ; Ruth Cave C ; Mónica Cornejo de L ; Sara Navarro V ; Marcel Deglin M ; Aída Milinarsky T ; Pilar Carvallo de SQ
  1. [1] Universidad de Valparíso Escuela de Medicina Laboratorio de Biología y Genética Molecular
• Localización: Revista Médica de Chile, ISSN-e 0034-9887, Vol. 130, Nº. 8, 2002, págs. 850-858
• Idioma: español
• Títulos paralelos:
  • Clinical and molecular genetic study of cystic fibrosis in the 5th Region of Chile
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• Resumen

  • Background: Cystic fibrosis (CF) is the most common autosomal recessive disease in Caucasian population. More than 900 mutations have been detected in the Cystic Fibrosis Transmembrane Regulator (CFTR) gene. The most common worldwide, is a deletion of phenylalanine 508 (deltaF508). Aim: To analyze the presence of mutations ∆F508, G542X, N1303K, G551D, R553X and S549N in patients from the 5th Region of Chile, with a clinical diagnosis of CF. Patients and methods: We studied 17 non-related patients, presenting frequent respiratory tract infections, malabsorption and positive sweat tests, or meconial ileum. Serum immunoglobulins (IgG, IgA, IgM), and total, CD3+ and B-lymphocytes, were determined to discard the presence of an immune deficiency. The molecular study of the gene was performed by Polymerase Chain Reaction amplification and restriction analysis. Results: Immunological parameters were normal in all patients. The deltaF508 mutation was detected in 11 chromosomes and the mutation G542X in 3 chromosomes. Conclusions: The mutation G542X was the second most frequent mutation found in this sample of Chilean CF patients. Since this mutation has a high frequency in Spanish CF patients, we suggest that this mutation might have had its origin in Spain (Rev Méd Chile 2002; 130: 850-8)