All Oklahoma babies are screened for:
Classical Galactosemia
Congenital Adrenal Hyperplasia (CAH)
Congenital Hypothyroidism
Cystic Fibrosis
Sickle Cell Anemia (HbSS Disease or HbS/Beta Zero Thalassemia) & Hemoglobin SC Disease (HbSC)
Biotinidase Deficiency
Hearing
Phenylketonuria (PKU)
Argininemia
Citrullinemia I, Argininosuccinic Acidemia, Citrullinemia II (Citrin Deficiency), PyruvateCarboxylase Deficiency
Maple Syrup (Urine) Disease
Homocystinuria (Cystathionine Beta-Synthase Deficiency [CBS Deficiency])
Tyrosinemia
Medium-chain Acyl-CoA Dehydrogenase (MCAD) Deficiency
Carnitine uptake Defect (CUD)
Short-Chain Acyl-CoA Dehydrogenase (SCAD) Deficiency & Glutaric Aciduria Type 2 (GA2)
Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
Carnitine Palmitoyltransferase 2 (CPT2) Deficiency & Acylcarnitine Translocase(CACT) deficiency
Carnitine Palmitoyl Transferase 1 Deficiency (CPT1)
Long-chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency (LCHADD) & Trifunctional Protein (TFP) Deficiency
Propionic Acidemia and Methylmalonic Acidemia
Glutaryl-CoA Dehydrogenase Deficiency (GA-1)
Organic Acidemias
Isovaleric Acidemia & 2-Methylbutyrylglycinuria
Malonic Aciduria
Isobutyryl-CoA Dehydrogenase Deficiency
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