When did cystic fibrosis newborn screening start
- how is cystic fibrosis diagnosed in babies
- how is cystic fibrosis detected in babies
- how is cystic fibrosis diagnosed in newborns
- how is cystic fibrosis diagnosed in children
Cystic fibrosis newborn screening false positive rate.
Cystic fibrosis
(SIS-tik • fie-BROH-suhs)
General Condition Information
Other Names
CF
Cystic fibrosis of the pancreas
Fibrocystic disease of the pancreas
Mucoviscidosis
Condition Type
Other Disorder
Birth Prevalence
- Hundreds of babies are born with this condition each year in the United States.
- Visit GeneReviews to learn more about how often this condition occurs.
Screening Finding
Increased immunoreactive trypsinogen (IRT) with or without at least one cystic fibrosis-causing change in the CFTR gene
What is cystic fibrosis
Cystic fibrosis is an inherited (genetic) condition that causes thick and sticky mucus to build up in the body.
Cystic fibrosis life expectancy
The thick mucus can lead to fluid-filled sacs (cysts) and scar tissue (fibrosis) in organs.
Cystic fibrosis results when a protein that controls how salt flows in and out of cells does not work properly. When salt doesn’t go where it needs to, levels of water in certain parts of the body are too high in some places and too low in others.
When mucus does not have enough water, it turns from thin and slipper
- how is cystic fibrosis diagnosed in toddlers
- how is cystic fibrosis diagnosed in infants