Literature DB >> 19457724

CFTR H609R mutation in Ecuadorian patients with cystic fibrosis.

María Rosa Moya-Quiles1, Guillermo Glover, Pedro Mondéjar-López, María Dolores Pastor-Vivero, Asunción Fernández-Sánchez, Manuel Sánchez-Solís.   

Abstract

Mutation epidemiology in each ethnic group is important for cystic fibrosis diagnosis and genetic counselling. To date, little has been reported on the prevalence of cystic fibrosis in the Ecuadorian population where the mutation distribution appears to differ from that of Europe. We present a series of four Ecuadorian patients homozygous for the H609R mutation in the CFTR gene. This is the first report of detection of this mutation in the Ecuadorian population. Taking advantage of the homozygous status of the patients, an evaluation of the most important clinical parameters is presented. From the diagnostic point of view, the information provided by our study is of relevance in designing an appropriate strategy for genetic testing of patients in Ecuador and in European countries where immigration from Ecuador is common.

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Year:  2009        PMID: 19457724     DOI: 10.1016/j.jcf.2009.05.001

Source DB:  PubMed          Journal:  J Cyst Fibros        ISSN: 1569-1993            Impact factor:   5.482


  4 in total

1.  Spectrum of CFTR gene mutations in Ecuadorian cystic fibrosis patients: the second report of the p.H609R mutation.

Authors:  Sofía C Ortiz; Santiago J Aguirre; Sofía Flores; Claudio Maldonado; Juan Mejía; Lilian Salinas
Journal:  Mol Genet Genomic Med       Date:  2017-10-11       Impact factor: 2.183

2.  Standardized clinical criteria and sweat test combined as a tool to diagnose Cystic Fibrosis.

Authors:  Fabricio González-Andrade
Journal:  Heliyon       Date:  2018-12-17

3.  Phenotyping Rare CFTR Mutations Reveal Functional Expression Defects Restored by TRIKAFTATM.

Authors:  Onofrio Laselva; Maria C Ardelean; Christine E Bear
Journal:  J Pers Med       Date:  2021-04-15

4.  Clinical, genetic and microbiological characterization of pediatric patients with cystic fibrosis in a public Hospital in Ecuador.

Authors:  Yazmina Lascano-Vaca; Esteban Ortiz-Prado; Lenin Gomez-Barreno; Katherine Simbaña-Rivera; Eduardo Vasconez; Alexander Lister; María Emilia Arteaga-Espinosa; Geovanny F Perez
Journal:  BMC Pediatr       Date:  2020-03-06       Impact factor: 2.125

  4 in total

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