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Stay tuned to upcoming events in the leukodystrophy newborn screening world.  Here, we will post information about webinars, conferences, and more that you may be interested in attending or watching.  And feel free to contact us if you have an event to share, too!

06Dec

Collaboration in Newborn Screening Advocacy is Essential

In the leukodystrophy space, we are seeing an increased amount of collaboration...

Rapid Whole Genome Sequencing at Rady Children's
01Dec

The Promise of Rapid Whole Genome Sequencing in Newborn Screening

  Rapid Whole Genome Sequencing may be the future for Newborn Screening,...

29Nov

What is a Newborn Screening Advisory Board?

If you’re just starting your Newborn Screening advocacy journey, one of the...

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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