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