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Indiana State Department of Health

Genomics Program Home > For Professionals > Newborn Screening Parent Toolkits Newborn Screening Parent Toolkits

Parent Toolkits

Click on one of the conditions below to print off the associated Parent ToolkitNOTE:  The Parent Toolkits below will print in both English & Spanish.  Please double-side print these files.

3-Methylcrotonyl-CoA carboxylase deficiency (3-MCC deficiency)

Amino acid (AA) disorders

Biotinidase deficiency

Fatty acid oxidation (FAO) disorders


Galactosemia variants


Medium chain acyl-CoA dehydrogenase (MCAD) deficiency

Maple syrup urine disease (MSUD)

Organic acid (OA) disorders

Phenylketonuria (PKU)