Agencies
Services
Metabolic Screening
Parent Information
- A Baby's First Step in Life: A Newborn Screening Guide for Parents - (En Español)
- Cystic Fibrosis: Information for Parents and Families
- Cystic Fibrosis: My Baby had a Positive CF Newborn Screening Test
- Disorder Information - (En Español)
- Hemoglobin C Trait
- Hemoglobin SC Disease
- Sickle Cell Beta Thalassemia Disease
- Sickle Cell Disease and Sickle Cell Carrier Status - (En Español)
- Newborn Metabolic Screening Disorder List
Fact Sheets for Physicians and Other Health Care Providers
- ALD Fact Sheet
- Beta Thalassemia Disease
- Biotinidase Deficiency
- Born Too Soon Premature Birth Information
- Congenital Adrenal Hyperplasia
- Congenital Hypothyroidism
- Cystic Fibrosis
- Fabry Disease
- Galactosemia
- Gaucher Disease
- Hemoglobin C Disease
- Hemoglobin D Disease (D-Los Angeles, D-Punjab, D-Ibadan)
- Hemoglobin E Disease
- Hemoglobin H Disease (Alpha Thalassemia)
- Hemoglobin SC Disease
- Homocystinuria
- Krabbe Disease
- Maple Syrup Urine Disease
- MCAD and Other Fatty Acid Oxidation Disorders
- Mucopolysaccharidosis Type I (MPS I) Disease (Hurler Syndrome)
- Mucopolysaccharidosis Type II (MPS II) Disease (Hunter Syndrome)
- Niemann Pick Disease
- Organic Acid Disorders
- Phenylketonuria
- Pompe Disease
- Severe Combined Immune Deficiency
- Sickle Cell Beta Thalassemia Disease
- Sickle Cell Disease
- Spinal Muscular Atrophy
- Tyrosinemia
- Urea Cycle Disorders
- 5-Oxoprolinuria (Glutathione synthetase deficiency)
