Cystic Fibrosis

Also known as:  Fibrocystic Disease of the Pancreas;  Mucoviscidosis;  Pancreas FibrocysticDisease;  Pancreatic Cystic Fibrosis;  Pancreatic Fibrosis;  Pulmonary Cystic Fibrosis

Cystic Fibrosis is a type of Nutrient Metabolism ailment caused by the inability of organic Chlorine (Chloride) ions to cross the Epithelial Cells of the body.  It occurs when an individual inherits two abnormal copies of the Gene that codes for the Chloride channel protein, Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) which is expressed in several organs including the Lungs, the Pancreas, the Biliary System, and the Sweat Glands.  Individuals with one normal and one defective Gene for this Protein are carriers of Cystic Fibrosis (able to pass it on to their offspring) but remain asymptomatic.

Cystic Fibrosis is usually fatal - the average lifespan of Cystic Fibrosis patients is 24 years.

 Cystic Fibrosis is the most common hereditary fatal disease afflicting Caucasians.

Digestive System

 Cystic Fibrosis may cause Pancreatic Insufficiency.

 Cystic Fibrosis may cause Steatorrhea.

Metabolism

 Cystic Fibrosis may cause increased susceptibility to Heat (due to the inability of Chloride ions to cross the epithelial cells of the perspiration glands).

Musculoskeletal System

 Cystic Fibrosis is characterized by the production of thick Mucous that obstructs the Intestinal Glands,Lugns, Pancreas and Bronchioles.

Respiratory System

        Bronchitis may occur as a complication arising from Cystic Fibrosis.

 Pneumonia may occur as a side effect of Cystic Fibrosis.