Newborn Screening Follow-up

CMA

3 Methylcrotonyl-CoA Carboxylase Deficiency

Acyl-CoA Dehydrogenase Deficiency

Deafness

Disorders of Fatty Acid Oxidation

Disorders of Folate Metabolism and Transport

Glycine Encephalopathy

Hearing Loss

Homocystinuria

Hypermethioninemia

Hyperphenylalaninemia

Hypothyroidism

Medium Chain Acyl-CoA Dehydrogenase Deficiency

Metabolism of Cobalamin, Folate and Homocysteine

Methylmalonic Acidemia

Methylmalonic Aciduria and Homocystinuria

Mucopolysaccharidosis

Neonatal Crisis/Illness

Organic Acidurias

Phenylalanine Hydroxylase Deficiency

Propionic Acidemia

Pyruvate Dehydrogenase Complex Deficiency

Thyroid Hormone Resistance

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