Nevada State Public Health Laboratory
The Nevada Newborn Screening Program ensures all babies are screened for certain disorders before they cause serious health problems. Many conditions are not easily recognizable at birth without proper testing. If left untreated, some disorders can cause mental retardation and even death. Newborn screening helps detect issues right after birth. When problems are found early, serious health conditions can be treated and prevented.
The newborn screening test is a simple, safe blood test performed shortly after the birth of your baby. A few drops of blood are taken from the baby's heel and put on special testing paper for analysis in our Nevada newborn screening lab located at the Nevada State Public Health Laboratory. The first test should be done between 24 and 26 hours of age or prior to discharge, whichever comes first. The second newborn screening should be done between 5 and 10 days of age, or at the baby's first doctor visit, whichever comes first.
The Nevada Newborn Screening Program screens infants for over 30 conditions, including metabolic disorders, endocrinal disorders, hematological disorders and cystic fibrosis.
Some of the Conditions Identified by Newborn Screening
- Congenital Hypothyroidism
- Phenylketonuria (PKU)
- Biotinidase Deficiency
- Congenital Adrenal Hyperplasia
- Amino Acid Disorders
- Fatty Acid/Organic Acid Disorders