Sanitas
Revista arbitrada de ciencias de la salud
Vol. 3(1), 32-38, 2024
Perspectivas en el abordaje científico de la fibrosis quística en la etapa pediátrica
Perspectives on the scientific approach to cystic fibrosis in paediatrics
Priscila Elizabeth Philco-Toaza
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6. Patricio Valle E, Burgos RI, Valle JR, Egas Bénar D, Ruiz Cabezas JC.
Analysis of CFTR gene mutations and cystic fibrosis incidence in the
Ecuadorian population. Invest Clin. 2007 marzo; 48(1): p. 91-98
7. Lascano-Vaca Y, Ortiz-Prado E, Gomez-Barreno L, Simbaña-Rivera K,
Eduardo Vasconez AL, Arteaga-Espinosa ME, et al. Clinical, genetic and
microbiological characterization of pediatric patients with cystic fibrosis in a
public Hospital in Ecuador. BMC Pediatrics. 2020; 20(111)
8. Zurita J, Sevillano G, González C, Lascano Y. Segniliparus rugosus from the
sputum of a child with cystic fibrosis in Ecuador: challenges in bacterial
identification. New Microbes New Infect. 2020;35:100668.
doi:10.1016/j.nmni.2020.100668
9. Paz-Y-Miño C, Zambrano AK, Ruiz-Cabezas JC, et al. Characterization of
Ancestral Origin of Cystic Fibrosis of Patients with New Reported Mutations
in CFTR. Biomed Res Int. 2020;2020:9074760. doi:10.1155/2020/9074760
10. Moya-Quiles MR, Glover G, Mondéjar-López P, Pastor-Vivero MD,
Fernández-Sánchez A, Sánchez-Solís M. CFTR H609R mutation in
Ecuadorian patients with cystic fibrosis. J Cyst Fibros. 2009;8(4):280-281.
doi:10.1016/j.jcf.2009.05.001
11. Valle EP, Burgos RI, Valle JR, Egas Béjar D, Ruiz-Cabezas JC. Analysis of
CFTR gene mutations and cystic fibrosis incidence in the Ecuadorian
population. Invest Clin. 2007;48(1):91-98.
12. Ortiz SC, Aguirre SJ, Flores S, Maldonado C, Mejía J, Salinas L. Spectrum of
CFTR gene mutations in Ecuadorian cystic fibrosis patients: the second report
of the p.H609R mutation. Mol Genet Genomic Med. 2017;5(6):751-757.
doi:10.1002/mgg3.337
13. Ruiz-Cabezas JC, Barros F, Sobrino B, et al. Mutational analysis of CFTR in
the Ecuadorian population using next-generation sequencing. Gene.
2019;696:28-32. doi:10.1016/j.gene.2019.02.015
14. González-Andrade F. Standardized clinical criteria and sweat test combined
as a tool to diagnose Cystic Fibrosis. Heliyon. 2018;4(12):e01050.
doi:10.1016/j.heliyon.2018.e01050
15. Paz-y-Miño C, Pérez JC, Burgos R, Dávalos MV, Leone PE. The DeltaF508
mutation in Ecuador, South America. Hum Mutat. 1999;14(4):348-350.
doi:10.1002/(SICI)1098-1004(199910)14:4<348:AID-HUMU11>3.0.CO;2-8
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