It is a genetic disease that is passed down through families that causes a thick, sticky mucus to build up in the lungs, digestive tract, and other areas of the body. It is caused by a defective gene where it does not produce the protein for the salt channels, resulting with the buildup of mucus. It is genetic, therefore there is no prevention of this disease. It is most common in Caucasians, and most is deadly. 1 in 29 Caucasians have the Cystic Fibrosis Gene. Blood Test Chest X-ray Lung Function Test Fecal Fat Test Sweat Chloride Test Air Comes through mouth/nose. Air goes down trachea & bronchi Salt channels maintain layer. Ends in alveoli Watery mucus layer helps trap & move debris. Air (O2) moves form alveoli to blood. Air Comes through mouth/nose. Salt channels maintain layer. Air goes down trachea & bronchi Genetic mutation causes salt channels to unevenly distribute salt and water across the layer of cells. Ends in alveoli Air (O2) moves form alveoli to blood. Thick mucus builds up in lungs, and eventually causing problems in digestive tract, and other areas. In Newborns: › Delayed growth › Failure to gain weight normally › No bowel movements in first 24-48 hours › Salty-tasting skin In the Bowel Functions: › Belly pain from severe constipation › Increased gas & bloating › Nausea & loss of appetite › Stool, that are pale or clay colored, foul smelling, and have mucus. Lungs & Sinuses › Coughing › Increases Mucus in the sinuses/lungs Weight loss Pneumonia Infertility Lungs: › Antibiotics to prevent & treat › › › › › lung & sinus infections Inhaled medicines DNA enzymes therapy Flu Vaccine Lung Transplant Oxygen Therapy Bowels: › Special diet high in protein & calories › Pancreatic enzymes to help absorb fats & proteins › Vitamin supplements Pictures are Hyperlinked! Sources of Information: http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0 001167/ http://people.usd.edu/~bgoodman/HotT.htm http://www.peds.ufl.edu/divisions/pulmonary/asth ma/normal-lung-function.asp http://learn.genetics.utah.edu/content/disorders/ whataregd/cf/