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Glossary of Cystic Fibrosis Terms-        Online Dictionary

Carrier

A person with one copy of a defective gene, who does not have the disease it causes, but can pass along the defective gene to offspring.

CFTR

Cystic fibrosis transmembrane conductance regulator, the protein responsible for regulating chloride movement across cells in some tissues. When a person has two defective copies of the CFTR gene, cystic fibrosis is the result.

Clubbing
 
Rounding and enlargement of fingers and toes
 

Gene Therapy

An evolving technique used to treat inherited diseases. The medical procedure involves either replacing, manipulating, or supplementing nonfunctional genes with healthy genes.

Pneumonia
 
Pneumothorax
 
Rupture of lung tissue and trapping of air between the lung and the chest wall
 
Pulmonary function tests
 
Pulmonary function tests measure how well the lungs take in and exhale air and how efficiently they transfer oxygen into the blood.
 

Emphysema

A pathological accumulation of air in organs or tissues; term especially applied to the condition when in the lungs.

Mucociliary escalator

The coordinated action of tiny projections on the surfaces of cells lining the respiratory tract, which moves mucus up and out of the lungs.

Mucolytic

An agent that dissolves or destroys mucin, the chief component of mucus.

Nasal polyps
 
Fleshy growths inside the nose
 

Pancreatic insufficiency

Reduction or absence of pancreatic secretions into the digestive system due to scarring and blockage of the pancreatic duct.

Sinusitis
 
Inflammation of the nasal sinuses, which are cavities in the skull behind, above, and on both sides of the nose
 
Lung transplantation
 
Lung transplant is surgery to replace one or both diseased lungs with healthy lungs from a human donor.

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