Literature DB >> 20683669

Past, present and future of newborn screening in Chile.

V Cornejo1, E Raimann, J F Cabello, A Valiente, C Becerra, M Opazo, M Colombo.   

Abstract

The history of the Newborn Screening Program in Chile begins in 1984, when a pilot plan was developed that demonstrated the feasibility of its implementation. In 1992, the Ministry of Health started a national newborn screening program for phenylketonuria (PKU) and congenital hypothyroidism (CH), and in 1998, this was extended to the entire country. Throughout this period, a total of 2,478,123 newborns (NB) have been analyzed, obtaining initial coverage of 48.8%, which was later increased to 87.7%, and at present it is at 98.7% of all NB of our country. During this period, 131 cases with PKU have been diagnosed, resulting in an incidence of 1:18,916 NB, an average age of diagnosis of 18 ± 10.2 days and average phenylalanine level of 19,9 ± 8.8 mg/dl. In relation to CH, 783 cases have been confirmed, arriving at an incidence of 1:3,163 NB, with average age of diagnosis of 12.5 ± 6.9 days. Due to the good results of the program, the government is evaluating the initiation of an extended pilot program, to introduce other pathologies.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20683669     DOI: 10.1007/s10545-010-9165-8

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  8 in total

1.  Medical genetics and genetic counseling in Chile.

Authors:  Sonia B Margarit; Mónica Alvarado; Karin Alvarez; Guillermo Lay-Son
Journal:  J Genet Couns       Date:  2013-06-07       Impact factor: 2.537

2.  Characterization of Phenyalanine Hydroxylase Gene Mutations in Chilean PKU Patients.

Authors:  V Hamilton; L Santa María; K Fuenzalida; P Morales; L R Desviat; M Ugarte; B Pérez; J F Cabello; V Cornejo
Journal:  JIMD Rep       Date:  2017-12-30

3.  Birth prevalence of phenylalanine hydroxylase deficiency: a systematic literature review and meta-analysis.

Authors:  Pamela K Foreman; Andrea V Margulis; Kimberly Alexander; Renee Shediac; Brian Calingaert; Abenah Harding; Manel Pladevall-Vila; Sarah Landis
Journal:  Orphanet J Rare Dis       Date:  2021-06-03       Impact factor: 4.123

Review 4.  Policy Making in Newborn Screening Needs a Structured and Transparent Approach.

Authors:  Marleen E Jansen; Karla J Lister; Henk J van Kranen; Martina C Cornel
Journal:  Front Public Health       Date:  2017-03-21

Review 5.  Metabolic etiologies in West syndrome.

Authors:  Seda Salar; Solomon L Moshé; Aristea S Galanopoulou
Journal:  Epilepsia Open       Date:  2018-03-14

Review 6.  Research, diagnosis and education in inborn errors of metabolism in Colombia: 20 years' experience from a reference center.

Authors:  Olga Y Echeverri; Johana M Guevara; Ángela J Espejo-Mojica; Andrea Ardila; Ninna Pulido; Magda Reyes; Alexander Rodriguez-Lopez; Carlos J Alméciga-Díaz; Luis A Barrera
Journal:  Orphanet J Rare Dis       Date:  2018-08-16       Impact factor: 4.123

7.  Global prevalence of classic phenylketonuria based on Neonatal Screening Program Data: systematic review and meta-analysis.

Authors:  Hamid Reza Shoraka; Ali Akbar Haghdoost; Mohammad Reza Baneshi; Zohre Bagherinezhad; Farzaneh Zolala
Journal:  Clin Exp Pediatr       Date:  2020-02-06

8.  Medical genetics and genomic medicine in Chile: opportunities for improvement.

Authors:  Silvia Castillo Taucher
Journal:  Mol Genet Genomic Med       Date:  2015-07       Impact factor: 2.183

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.