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Michigan Newborn Screening Brochure – English

This MDHHS brochure on the Newborn Screening Program explains the screening process, why it is done, and what happens if it suggests a potential health problem.

Link to resource:
https://www.michigan.gov/mdhhs/-/media/Project/Websites/mdhhs/Adult-and-Childrens-Services/Children-and-Families/Hereditary-Disorders/Newborn-Screening/newborn_screening_broc_110897_7.pdf?rev=bb0c7d6812b1448f98db7c418c945480&hash=F6B4AC07C740E6FE9AA99D7063E523D3
Audience: Patients and Families, Providers
Languages: Arabic, English, Spanish
Keywords: 3mcc, amino acid disorders, arg, argininemia, asa, bio, biotinidase deficiency, cah, carnitine uptake disorders, cf, ch, cit, citrullinemia, cystic fibrosis, ehdi, endocrine disorders, faod, fatty acid oxidation disorders, galactosemia, galt, hcy, hearing deficiency, hemoglobinopathies, homocystinuria, lchad, m/schad, maple syrup urine disease, mcad, metabolic disease, msud, NBS, Newborn Screening, organic acid disorders, pa, phenylketonuria, pku, propionic acidemia, Resource, scad, scid, thalassemias, trifunctional protein deficiency, tyrosinemia, vlcad
←Center for Medicare and Medicaid Services – Medicare
Michigan Newborn Screening Brochure – Arabic→

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