Neonatal Chemistry

Kansas Panel of Newborn Disorders

Amino Acid Disorders Phenylketonuria   Maple Syrup Urine Disease   Homocystinuria   Tyrosinemia   Argininosuccinic Aciduria   Citrullinemia   Organic Acid Disorders Isovaleric Acidemia   Glutaric Acidemia Type I   HMG-CoA lyase Deficiency   Multiple Carboxylase Deficiency   Methylmalonic Acidemia-Mutase Deficiency   Methylmalonic Acidemias A & B   3-Methylcrotonyl-CoA Carboxylase Deficiency   Propionic Acidemia   Beta-Ketothiolase Deficiency

Fatty Acid Disorders Medium-Chain Acyl-CoA Dehydrogenase Deficiency   Very Long-Chain Acyl-CoA Dehydrogenase Deficiency   Long-Chain 3-OH Acyl-CoA Dehydrogenase Deficiency   Trifunctional Protein Deficiency   Carnitine Uptake Defect   Additional Disorders Hemoglobinapothies   Sickle Cell   Beta Thalassemia   Galactosemia   Biotinidase Deficiency   Congenital Hypothyroidism   Congenital Adrenal Hyperplasia   Cystic Fibrosis   Kansas Information Sheets for Parents KS Information for Parents