Fact Sheets for Results/Conditions
Downloads
- Absent Biotinidase Activity (Possible Biotinidase Deficiency)
- Alpha Thalassemia Trait
- Borderline Results (Repeat Screening Needed)
- Critical Congenital Heart Disease – English
- Critical Congenital Heart Disease – Spanish
- Decreased Biotinidase Activity (Possible Biotinidase Deficiency)
- Decreased GALT Activity (Possible Galactosemia Variant)
- Very Low GALT Activity (Possible Galactosemia)
- Elevated TSH (Possible Congenital Hypothyroidism)
- Elevated C3 (Possible Organic Acid Disorder)
- Elevated C5 (Possible Isovaleric Acidemia)
- Elevated C5DC (Possible Glutaric Acidemia Type 1)
- Elevated C5OH (Possible Organic Acid Disorder)
- Elevated Citrulline (Possible Urea Cycle Disorder)
- Elevated Leucine (Possible Maple Syrup Urine Disease)
- Elevated Methionine (Possible Homocystinuria)
- Elevated Phenylalanine (Possible Phenylketonuria)
- Elevated Tyrosine (Possible Tyrosinemia)
- Fatty Acid Oxidation Disorders
- Hemoglobin C Disease
- Hemoglobin C Trait
- Hemoglobin D Trait
- Hemoglobin E Disease
- Hemoglobin E Trait
- Newborn Screening Triple Threat Fact Sheet – English
- Newborn Screening Triple Threat Fact Sheet – Spanish
- Preliminary High 17-OHP (Possible Congenital Adrenal Hyperplasia)
- Positive mutation Analysis (Possible Cystic Fibrosis)
- Positive Steroid Profile (Possible Congenital Adrenal Hyperplasia)
- Severe Combined Immunodeficiency Disease (SCID)
- Sickle Cell Trait
- Sickle-Beta Thalassemia
- Sickle-Hemoglobin C Disease
- Sickle-Hemoglobin E Disease
- Trait for Unidentified Hemoglobin
- X-Linked Adrenoleukodystrophy (X-ALD) Disorder
