AllRefer Health - Neonatal Cystic Fibrosis Screening (Cystic Fibrosis Screening - Neonatal, Immunoreactive Trypsinogen)

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You are here : AllRefer.com > Health > Tests & Exams > Neonatal Cystic Fibrosis Screening

Neonatal Cystic Fibrosis Screening


•	Definition
•	Why is the Test Performed?
•	How is the Test Performed?
•	How to Prepare for the Test?
•	How will the Test Feel?
•	Normal Values
•	What do Abnormal Results Mean?
•	Risks
•	Pictures & Images
•	Go To Main Page

Alternate Names : Cystic Fibrosis Screening - Neonatal, Immunoreactive Trypsinogen

Definition

Neonatal cystic fibrosis screening involves a pancreatic test that evaluates immunoreactive trypsinogen. The test is performed on newborns to determine whether the baby has cystic fibrosis (CF).

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Infant Blood Sample

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Why is the Test Performed?

Cystic fibrosis is a genetic disease that affects the sweat glands as well as the respiratory and gastrointestinal systems. Trypsinogen is produced by the pancreas and is elevated in babies with cystic fibrosis. This test is a screening tool to identify infants who need further testing to confirm the diagnosis.

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• Definition
• Why is the Test Performed?
• How is the Test Performed?
• How to Prepare for the Test?
• How will the Test Feel?
• Normal Values
• What do Abnormal Results Mean?
• Risks
• Pictures & Images

Review Date : 11/3/2002
Reviewed By : Philip L. Graham III, M.D., F.A.A.P., Department of Pediatrics, Children's Hospital of New York, Columbia University, New York, NY. Review provided by VeriMed Healthcare Network.

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