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Glucose-6-Phosphate dehydrogenase deficiency incidence in a Hispanic population.
Cantú-Reyna, C; Santos-Guzmán, J; Cruz-Camino, H; Vazquez Cantu, D L; Gómez-Gutiérrez, R; Góngora-Cortéz, J J; Gutiérrez-Castillo, A.
Affiliation
  • Cantú-Reyna C; Genomi-k S.A.P.I. de C.V., Monterrey, Nuevo León, Mexico.
  • Santos-Guzmán J; Tecnologico de Monterrey, Escuela de Medicina y Ciencias de la Salud, Monterrey, Nuevo León, Mexico.
  • Cruz-Camino H; Tecnologico de Monterrey, Escuela de Medicina y Ciencias de la Salud, Monterrey, Nuevo León, Mexico.
  • Vazquez Cantu DL; Genomi-k S.A.P.I. de C.V., Monterrey, Nuevo León, Mexico.
  • Gómez-Gutiérrez R; Tecnologico de Monterrey, Escuela de Ingeniería y Ciencias, Monterrey, Nuevo León, Mexico.
  • Góngora-Cortéz JJ; Tecnologico de Monterrey, Escuela de Medicina y Ciencias de la Salud, Monterrey, Nuevo León, Mexico.
  • Gutiérrez-Castillo A; Genomi-k S.A.P.I. de C.V., Monterrey, Nuevo León, Mexico.
J Neonatal Perinatal Med ; 12(2): 203-207, 2019.
Article de En | MEDLINE | ID: mdl-30741698
ABSTRACT
Glucose-6-phosphate dehydrogenase deficiency (D-G6PD) is a common erythroenzymopathy that needs to be addressed as an important public health issue. Proper population monitoring is needed to anticipate clinical complications. A joint venture between Genomi-k (a Mexican company focused on newborn screening) and several university researchers conducted a retrospetive study for D-G6PD based on 156,152 newborn screening reports belonging to the Mexican population comprising a period of 10 years. We identified 540 male newborns affected with this deficiency, representing an incidence of 6.78 cases per 1,000 newborn males. A single double mutation of G202AA376G was detected in 97.22% of cases. In regions where there is an absence of a national centralized health data for D-G6PD, information from a non-probabilistic large population sample can be used as a national incidence subrogate.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Déficit en glucose-6-phosphate-déshydrogénase Type d'étude: Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limites: Humans / Male / Newborn Pays/Région comme sujet: Mexico Langue: En Journal: J Neonatal Perinatal Med Année: 2019 Type de document: Article Pays d'affiliation: Mexique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Déficit en glucose-6-phosphate-déshydrogénase Type d'étude: Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limites: Humans / Male / Newborn Pays/Région comme sujet: Mexico Langue: En Journal: J Neonatal Perinatal Med Année: 2019 Type de document: Article Pays d'affiliation: Mexique