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Newborn Screening - List of Disorders
All infants born in Michigan are screened for 50+ disorders and hearing. Shown below are the disorders included on the screening panel. (Fact sheets are available for some disorders.)
Disorders Coming Soon: The following condition has been approved for Michigan's panel but implementation is in progress and screening has not yet begun.
- Guanidinoacetate methyltransferase (GAMT) deficiency
**Over 1800 mutations have been identified in the gene associated with Cystic Fibrosis, the Cystic Fibrosis Transmembrane Regulator (CFTR) gene. Most newborn screening programs only screen for the most common disease causing CFTR gene mutations.