Health services use by children identified as heterozygous hemoglobinopathy mutation carriers via newborn screening

BACKGROUND: Newborn screening (NBS) for sickle cell disease incidentally identifies heterozygous carriers of hemoglobinopathy mutations. In Ontario, Canada, these carrier results are not routinely disclosed, presenting an opportunity to investigate the potential health implications of carrier status...

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Bibliografiske detaljer
Udgivet i:BMC Pediatr
Main Authors: Khangura, Sara D., Potter, Beth K., Davies, Christine, Ducharme, Robin, Bota, A. Brianne, Hawken, Steven, Wilson, Kumanan, Karaceper, Maria D., Klaassen, Robert J., Little, Julian, Simpson, Ewurabena, Chakraborty, Pranesh
Format: Artigo
Sprog:Inglês
Udgivet: BioMed Central 2021
Fag:
Research
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC8247172/
https://ncbi.nlm.nih.gov/pubmed/34210267
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12887-021-02751-8
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