The Leukodystrophy Newborn Screening Action Network is a coalition of leukodystrophy patient advocates dedicated to championing the cause of newborn screening for leukodystrophies and lysosomal storage disorders. 

Head Office

Philadelphia, PA 19031

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    3-Hydroxy-3-Methylglutaric Aciduria
    3-Methylcrotonyl-CoA Carboxylase Deficiency
    Argininosuccinic Aciduria
    Beta-Ketothiolase Deficiency
    Biotinidase Deficiency
    Carnitine Uptake Defect
    Citrullinemia, Type I
    Classic Galactosemia
    Classic Phenylketonuria
    Congenital Adrenal Hyperplasia
    Critical Congenital Heart Disease
    Cystic Fibrosis
    Glutaric Acidemia, Type I
    Hearing loss
    Hemoglobinopathies
    Holocarboxylase Synthetase Deficiency
    Homocystinuria
    Isovaleric Acidemia
    Long-Chain L-3 Hydroxyacyl-CoA Dehydrogenase Deficiency
    Maple Syrup Urine Disease
    Medium-Chain Acyl-CoA Dehydrogenase Deficiency
    Methylmalonic Acidemia (Cobalamin Disorders)
    Methylmalonic Acidemia (Methymalonyl-CoA Mutase Deficiency)
    Primary Congenital Hypothyroidism
    Propionic Acidemia
    S, Beta-Thalassemia
    S, C Disease
    Severe Combined Immunodeficiency
    Sickle Cell Anemia
    Trifunctional Protein Deficiency
    Tyrosinemia, Type I
    Very Long-Chain Acyl-CoA Dehydrogenase Deficiency
    Adrenoleukodystrophy