Provider Action Sheets
The Kansas Newborn Screening Program has modified the following items which are included in the American College of Medical Genetics and Genomics (ACMG) Intermediate Management Guide:
- ACTion (ACT) sheets that describe the short term actions a health professional should follow in communicating with the family and determining the appropriate steps in the follow-up of the infant that has screened positive
- Algorithms that present an overview of the basic steps involved in determining the final diagnosis of the infant
- View Guide Documents.
Disorder Type | Conditions |
|---|---|
Hemoglobinopathies | |
Hemoglobin SC disease (HbSC) Algorithm | ACT Sheet | Info Sheet | |
Hemoglobin S/beta Thalassemia (HbSß+) Algorithm | ACT Sheet | Info Sheet | |
Sickle cell carrier (trait) (HbAS) Algorithm | ACT Sheet | Info Sheet | |
Other Disorders | Congenital Hypothyroidism (CH) |
Biotinidase Deficiency (BIO) | |
Congenital Adrenal Hyperplasia (CAH) | |
Galactosemia (GALT) | |
Cystic Fibrosis (CF) | |
HEAR Algorithm | ACT Sheet | Info Sheet | |
Severe Combined Immune Deficiency (SCID) | |
Spinal Muscular Atrophy (SMA) | |
Critical Congenital Heart Defect (CCHD) Algorithm | ACT Sheet | Info Sheet | |
Amino Acid Disorders | Phenylketonuria (PKU) |
Maple Syrup Urine Disease (MSUD) | |
Homocystinuria (HCY) | |
Tyrosinemia (TYR) | |
Argininosuccinic Aciduria (ASA) | |
Citrullinemia, Type 1 (CIT) Algorithm | ACT Sheet | Info Sheet | |
Fatty Acid Disorders | Medium-Chain Acyl-Coa Dehydrogenase Deficiency (MCAD) |
Very Long-Chain Acyl-CoA Dehydrogenase Deficiency (VLCAD) | |
Long-Chain L-3 Hydroxyacyl-CoA Dehydrogenase Deficiency (LCHAD) | |
Trifunctional Protein Deficiency (TFP) Algorithm | ACT Sheet | Info Sheet | |
Carnitine Uptake Defect (CUD) | |
Organic Acid Disorders | Isovaleric Acidemia (IVA) |
Glutaric Acidemia, Type 1 (GA-I) | |
3-Hydroxy-3-Methylglutaric Aciduria (HMG) | |
Holocarboxyalse Synthetase Deficiency (MCD) Algorithm | ACT Sheet | Info Sheet | |
Methylmalonic Acidemia (Methymalonyl-CoA Mutase Deficiency) (MUT) | |
Methylmalonic Acidemia (Cobalamin Disorders) (Cbl A, B) Algorithm | ACT Sheet | Info Sheet | |
3-Methylcrotonyl-CoA Carboxylase Deficiency (3MCC) Algorithm | ACT Sheet | Info Sheet | |
Propionic Acidemia (PROP) Algorithm | ACT Sheet | Info Sheet | |
Beta-Ketothiolase Deficiency (BKT) Algorithm | ACT Sheet | Info Sheet |