Newborn blood spot screening for galactosemia, tyrosinemia type I, homocystinuria, sickle cell anemia, sickle cell/beta-thalassemia, sickle cell/hemoglobin C disease, and severe combined immunodeficiency
Autor: | Waye, Arianna, El Shayeb, Mohamed, Guo, Bing, Chuck, Anderson, Akpinar, Ilke, Chojecki, Dagmara, Yan, Charles, Corabian, Paula |
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Jazyk: | angličtina |
Předmět: | |
Zdroj: | Education and Research Archive. |
Popis: | This STE report examines the safety, screening accuracy, therapeutic efficacy/effectiveness, cost-effectiveness, budget impact, and health system readiness of newborn screening for seven conditions (galactosemia, tyrosinemia type I, homocystinuria, sickle cell anemia, sickle cell/beta-thalassemia, sickle cell/hemoglobin C disease, and severe combined immunodeficiency), contextualized to the Alberta setting. |
Databáze: | OpenAIRE |
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