Screens all
infants born within the State of Arizona for eight genetic disorders:
biotinidase deficiency, congenital hypothyroidism, galactosemia,
homocystinuria, maple syrup urine disease, phenylketonuria, sickle cell
disease, and congenital adrenal hyperplasia. Early detection of these
disorders provides faster treatment, reducing the chances of serious mental
impairment or other harmful physical effects. Contact (602) 542-1184 for
specific questions on test methods and specimen rejection criteria.
Collection
Procedures
Please visit this page for visuals and descriptions of the proper
collection procedure. Representatives from the State Lab will also visit
facilities to provide on site training. Please contact us to set up this
service.
Related Links
Links to helpful websites for additional Newborn Screening information. |
