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Laboratories
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Neonatal Chemistry
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Kansas Panel of Newborn Disorders
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