Wyoming’s Newborn Screening Panel

 

Endocrine Disorders

1.  Congenital Adrenal Hyperplasia (CAH)

2.  Congenital Hypothyroidism (CH)

Genetic

3.  Biotinidase Deficiency (BIOT)

4.  Cystic Fibrosis (CF)

5.  Hearing (HEAR), this screen is not a metabolic/bloodspot screen

Hemoglobinopathies

6. Sickle β-Thalassemia (Hb S/β Th)

7. Sickle Cell Anemia (Hb SC)

8. Sickle S (Hb SS)

Metabolic

9. Galactosemia (GALT)

10. Phenylketonuria (PKU)

Amino Acid Disorders

11. Argininosuccinic Acidemia (ASA)

12. Citrullinemia (CIT)

13. Homocystinuria (HCY)

14. Maple Syrup Urine Disease (MSUD)

15. Tyrosinemia (TYR 1)

Fatty Acid Oxidation Disorders

16. Carnitine Uptake Defect (CUD)

17. Long-chain L-3-OH acyl-CoA Dehydrogenase Deficiency (LCHAD)

18. Medium-chain acyl-CoA Dehydrogenase Deficiency (MCAD)

19. Trifunctional Protein Deficiency (TFP)

20. Very long-chain acyl-CoA Dehydrogenase Deficiency (VLCAD)

Organic Acid Disorders

21. 3-Hydroxy 3-Methyl Glutaric Acid (HMG)

22. 3-Methylcrotonyl-CoA Carboxylase Deficiency (3MCC)

23. β-Ketothiolase Deficiency (BKT)

24. Glutaric Acidemia Type 1 (GA1)

25. Isovaleric Acidemia (IVA)

26. Methylmalonic Acidemia – Mutase Deficiency (MUT)

27. Methylmalonic Acidemia (Cbl, A, B)

28. Multiple Carboxylase Deficiency (MCD)  

29. Propionic Acidemia (PROP)