Literature DB >> 33462772

Neonatal screening program for five conditions in Honduras.

Michelle Melissa Miralda Buckley1, Lindsay Borjas Aguilar2, Rosibel Colindres Lainez3, Hector Joaquin Alvarado Valenzuela3, Fernando Ponce4, Débora Gusmão Melo5,6,7.   

Abstract

We present the initial results of a neonatal screening program in part of the public health system in Honduras, that is, the Honduran Social Security Institute. The program design includes steps from neonatal bloodspot in the first newborn days to evaluation and treatment when necessary. In 2018 and 2019, 19,911 newborns were tested for hypothyroidism, cystic fibrosis, galactosemia, phenylketonuria, and adrenal hyperplasia. Abnormalities were identified in 18 newborns, corresponding to a prevalence of 9:10,000. Considering all births in Honduras, the estimated coverage of screening ranged between 4.4 and 5.7%. These results reinforce the need to expand and consolidate neonatal screening.

Entities:  

Keywords:  Birth defects; Honduras; Inborn errors of metabolism; Neonatal screening

Year:  2021        PMID: 33462772     DOI: 10.1007/s12687-021-00506-7

Source DB:  PubMed          Journal:  J Community Genet        ISSN: 1868-310X


  4 in total

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  4 in total

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