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Louisiana Department of Health & Hospitals | Kathy Kliebert, Secretary

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Statewide Initiatives



211 - Get Connected. Get Answers.

Newborn Screening Disorders

Amino Acid Metabolism Disorders

  • Argininosuccinic Aciduria (ASA)
  • Citrullinemia (CIT)
  • Homocystinuria (HCY)
  • Phenylketonuria (PKU)
  • Maple Syrup Urine Disease (MSUD)
  • Tyrosinemia (TYR)

Biotinidase Deficiency
Congential Adrenal Hyperplasia (CAH)
Congential Hypothyroidism (CH)
Cystic Fibrosis (CF)
Fatty Acid Oxidation Disorders

  • Carnitine Uptake Deficiency (CUD)
  • Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)
  • Long-chain L-3-OH acyl-CoA Dehydrogenase Deficiency (LCHAD)
  • Very Long-Chain acyl-CoA Dehydrogenase Deficiency (VLCAD)
  • Trifunctional Protien Deficiency (TFP)

Classical Galactosemia (GALT)
Hemoglobinopathies

  • Sickle Cell Anemia (Hb SS)
  • Hb S/ß-thalassemia (Hb S/ß Th)
  • Hb S/C diease (Hb S/C)

Organic Acidemia Disorders

  • ß-Ketothiolase deficienct (BKT)
  • Glutaric Acidemia type I (GA I)
  • 3-OH 3-CH3 Glutaric Aciduria (HMG)
  • Isovaleric Acidemia (IVA)
  • Methylmalonic Acidemia -Cbl A, B (Cbl A, B)
  • Methylmalonic Acidemia mutase deficiency (MUT)
  • 3-Methylcrotonyl-CoA carboxylase Deficiency (3MCC)
  • Multiple carboxylase Deficiency (MCD)
  • Propionic Acidemia (PA)