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Michigan Newborn Screening Program

This public health program, required by Michigan Law, helps find babies with rare but serious medical conditions that require early treatment.

Link to resource:
http://www.michigan.gov/mdch/0,1607,7-132-2942_4911_4916-64851--,00.html
Audience: Patients and Families, Providers
Languages: English
Keywords: 3mcc, amino acid disorders, arg, argininemia, asa, bio, biotinidase deficiency, cah, carnitine uptake disorders, cf, ch, cit, citrullinemia, cystic fibrosis, ehdi, faod, fatty acid oxidation disorders, follow up, galactosemia, galt, Genetic Disorders, Genetic Testing, hcy, health outcomes, hearing deficiency, hemoglobinopathies, homocystinuria, Labs, Law, lchad, m/schad, maple syrup urine disease, mcad, metabolic disorders, msud, NBS, Newborn Screening, organic acid disorders, pa, phenylketonuria, pku, positive, propionic acidemia, scad, scid, thalassemias, trifunctional protein deficiency, tyrosinemia, vlcad
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