Newborn Screening Testing at SHL

The State Hygienic Laboratory is CLIA accredited to perform laboratory screening tests for over 50 inherited genetic/metabolic conditions on all infants born in Iowa. The laboratory works round the clock, 365 days a year to ensure that conditions are identified, and lifesaving treatments can be provided so that babies can thrive.  SHL partners with the University of Iowa Stead Family Children’s Hospital, for provider consultation, genetic counseling, and follow-up services.   

  • Screening tests may identify increased risk for the following conditions: amino acid disorders, biotinidase deficiency, congenital adrenal hyperplasia, cystic fibrosis, fatty acid oxidation disorders, galactosemia, hemoglobinopathies, hypothyroidism,  Pompe Disease, Mucopolysaccharidosis Type 1, and X-linked Adrenoleukodystrophy, and organic acid disorders. 

  • The child's licensed health-care provider will be informed when the tests are completed and if results warrant further

Collection Instructions

NBS Collection Manifest

Contact

Ken Coursey, Clinical Lab Manager

Title/Position
Newborn Screening