States Tennessee
Conditions Screened
Tennessee currently screens for 68 conditions
The Tennessee Program
Each state runs its program differently, for more detailed information please visit their website here.
Download Brochure
Here is a brochure for the state of Tennessee. Brochure »
What Conditions are Screened For in Tennessee?
Amino Acid Disorders
-
Argininemia (ARG)
-
Benign Hyperphenylalaninemia (H-PHE)
-
Biopterin Defect in Cofactor Biosynthesis (BIOPT-BS)
-
Biopterin Defect in Cofactor Regeneration (BIOPT-REG)
-
Citrullinemia, Type I (CIT)
-
Citrullinemia, Type II (CIT II)
-
Classic Phenylketonuria (PKU)
-
Homocystinuria (HCY)
-
Hypermethioninemia (MET)
-
Hyperornithine with Gyrate Deficiency (Hyper ORN)
-
Maple Syrup Urine Disease (MSUD)
-
Tyrosinemia, Type I (TYR I)
-
Tyrosinemia, Type II (TYR II)
-
Tyrosinemia, Type III (TYR III)
Endocrine Disorders
Fatty Acid Oxidation Disorders
-
2,4 Dienoyl-CoA Reductase Deficiency (DE RED)
-
Carnitine Uptake Defect (CUD)
-
Glutaric Acidemia, Type II (GA-2)
Hemoglobin Disorders
-
Hemoglobinopathies (Var Hb)
-
S, Beta-Thalassemia (Hb S/ßTh)
-
S, C Disease (Hb S/C)
-
Sickle Cell Anemia (Hb SS)
Lysosomal Storage Disorders
-
Fabry (FABRY)
-
Gaucher (GBA)
-
Mucopolysaccharidosis Type-I (MPS I)
-
Pompe (POMPE)
Organic Acid Conditions
-
2-Methyl-3-Hydroxybutyric Acidemia (2M3HBA)
-
2-Methylbutyrylglycinuria (2MBG)
-
3-Methylglutaconic Aciduria (3MGA)
-
Glutaric Acidemia, Type I (GA-1)
-
Isobutyrylglycinuria (IBG)
-
Isovaleric Acidemia (IVA)
-
Malonic Acidemia (MAL)
-
Methylmalonic Acidemia with Homocystinuria (Cbl C, D, F)
-
Propionic Acidemia (PROP)
Other Disorders
-
Adrenoleukodystrophy (ALD)State preferred name: X-Linked Adrenoleukodystrophy (ALD)
-
Biotinidase Deficiency (BIOT)
-
Classic Galactosemia (GALT)
-
Cystic Fibrosis (CF)
-
Galactoepimerase Deficiency (GALE)
-
Galactokinase Deficiency (GALK)
-
Hearing loss (HEAR)
-
Spinal Muscular Atrophy (SMA)
Search Educational Resources
Looking for resources? Check out our Newborn Screening Education and Training Resource Center.
About Newborn Screening in Tennessee
Program Overview:
Tennessee has a comprehensive genetics program that provides access to genetic screening, diagnostic testing, and counseling services for individuals and families who have, or are at risk for, genetic conditions. These comprehensive screening programs provide a public health service for the citizens of Tennessee.
Newborn screening allows for early diagnosis of metabolic conditions, followed by appropriate medical treatment. All babies born in Tennessee are screened for certain genetic conditions. If any of the tests are abnormal, which mean they are indicating a possible disorder, the Department of Health follows up with the baby’s doctor to initiate retesting, confirmation and treatment from a specialist if necessary.
Early diagnosis and treatment can make the difference between a child leading a relatively normal life or having more significant developmental delays, long-term health care needs, or even death.
How is Newborn Screening Paid for in Tennessee?
The newborn screening cost is $185.00 per child payable to the Department of Health. The fee is waived for patients who are unable to pay based on information at the time of admission to the healthcare facility.
Policies and Resources
Opt-Out:
All newborns must participate in newborn screening unless a parent or guardian objects on religious grounds. Parents who decline must sign a written refusal statement.
Support for families:
Additionally, the Children Special Services (CSS) Program provides services to eligible children with special health care needs. CSS has two components; medical services and care coordination.
The first component provides for reimbursement of medical services, i.e., physician/clinic visits, hospitalizations, medical supplies, pharmaceuticals, durable medical equipment, and therapies for children from birth to age 21 years who meet medical and financial eligibility requirements.
The second component is care coordination. CSS coordinates primary and specialty care through the designated primary care physician and corresponding managed care organization networks. Care coordinators assist the family in accessing many services (educational, medical, social, transportation, support and advocacy).
For more information about your child’s eligibility for CSS, please contact Family Health and Wellness. The office is located in the Andrew Johnson Tower, 710 James Robertson Parkway, 8th Floor, Nashville, TN 37243. You may also call the program at (615) 741-7353.
Storage and Use of Dried Blood Spots:
After your child’s blood has been screened for all newborn screening conditions, some blood will remain in the sample card. This is called a “residual dried blood spot”. In Tennessee, the residual dried blood spot will be retained by the state for 12 months if the sample was negative, while confirmed tests are held indefinitely.
To see a copy of the blood spot card used in Tennessee, click here.
Was this Helpful?
Your input helps us improve the site for parents and practitioners. Leave us feedback about this page.
Was this page helpful?