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Newborn Screening Home | Health Professionals Guide | Parents Guide | Disorders Tested | Statistics | Publications/Newsletter | Educational Brochures | Advisory Committee | Site Map
Site Map
- WISCONSIN HEALTH CARE PROFESSIONALS' GUIDE
TO NEWBORN SCREENING
- Introduction
- The Test Panel and Timeline
- When to Collect a Blood Sample
- How to Collect a Blood Sample
- Collection Card Ordering and Pricing
- Wisconsin Newborn Screening Card
- Sample Handling and Mailing
- Laboratory Testing and Reporting
- Sample Acceptability
- Treatment Centers
- Desription of Disorders
- Newborn Screening Statute
- Newborn Screening Funding
- Wisconsin Newborn Screening Advisory Group
- Newborn Screening Program Administration
- PARENT'S PAGE
- What is the Newborn Screening Program?
- Newborn Screening is Required
- How Is the Screening Done?
- How Will I Get The Results?
- Newborn Screen Results
- Repeating the Newborn Screen
- The Newborn Screening Disorders
- Where to Get More Information
- DISORDERS
- Argininosuccinic Acidemia (ASA)
- Biotinidase Deficiency
- Citrullinemia (Type I & II)
- Congenital Adrenal Hyperplasia
- Congenital Hypothyroidism
- Cystic Fibrosis
- Fatty Acid Oxidation (12)
- Galactosemia
- Hearing Screening
- Hemoglobin S-Beta Thalassemia
- Hemoglobin S/C Disease
- Hemoglobin Variants
- Homocystinuria
- Hypermethioninemia
- Hyperphenylalaninemia
- Maple Syurp Urine Disease
- Organic Acidemia (15)
- Phenylketonuria
- Sickle Cell Disease
- Tyrosinemia (Type I, II & III)
- LINKS TO RELATED SITES
- Links Page
- NEWBORN SCREENING PUBLICATIONS
- Newsletters
- Educational Brochures
- STATISTICS
- Number of Confirmed Cases by Disorder
- Number and Cause of Unsatisfactory Samples
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