Newborn Screening for Metabolic and Sickle Cell Disorders Program

Disorders

Newborns are tested for early signs of the following conditions:

3-Methylcrotonyl-CoA Carboxylase Deficiency (3MCC)

Argninosuccinic aciduria

Beta-ketothiolase deficiency

Biotinidase Deficiency

Carnitine Uptake Defect

Citrullinemia

Congenital Adrenal Hyperplasia

Cystic Fibrosis

Galactosemia

Glutaric Acidemia Type I

3-OH 3-CH3 Glutaric Aciduria (HMG)

Sickle Cell Disease and other hemoglobin conditions (3 types)

Homocystinuria

Hypothyroidism

Isovaleric Acidemia

Long-chain L-3-OH Acyl-CoA Dehydrogenase Deficiency (LCHAD)

Maple Syrup Urine Disease (MSUD)

Medium Chain Acyl Co-A Dehydrogenase Deficiency (MCADD)

Methylmalonic Acidemias (2 types)

Multiple Carboxylase Deficiency

Phenylketonuria (PKU)

Propionic Acidemia

Trifunctional Protein Deficiency

Tyrosinemia

Very Long-Chain Acyl-CoA Dehydrogenase Deficiency (VLCAD)

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