Cystic Fibrosis
Cystic Fibrosis Foundation: Home
The CF Foundation is the world's leader in the fight against CF, and our scientific portfolio reflects our drive to provide effective treatments and — one day — ...
Cystic fibrosis - Symptoms and causes - Mayo Clinic
What is cystic fibrosis? A Mayo Clinic expert explains. Learn more from pulmonologist Sarah Chalmers, MD.
Learn how the cystic fibrosis transmembrane conductance regulator affects the digestive system. Watch this video to see how we count our success in lives.
Cystic Fibrosis: Causes, Symptoms & Treatment - Cleveland Clinic
Cystic Fibrosis. Cystic fibrosis (CF) is a genetic (inherited) disease that causes sticky, thick mucus to build up in organs, including the lungs and the ...
What Is Cystic Fibrosis? | NHLBI, NIH
Cystic fibrosis is a life-shortening inherited condition that affects a certain protein called CFTR in the body.
CF is a rare genetic disorder that affects mostly the lungs, but also the pancreas, liver, kidneys, and intestine. ... The hallmark feature of CF is the ...
Key points · Cystic fibrosis (CF) is a genetic disorder that causes problems with breathing and digestion. · People who are pregnant or planning ...
Cystic Fibrosis | Johns Hopkins Medicine
Detailed information on cystic fibrosis, including symptoms, diagnosis, treatment, and geneticsture to Product Detail Pages: POST LAUNCH ( retainer )
Cystic fibrosis: MedlinePlus Genetics
Cystic fibrosis is an inherited disease characterized by the buildup of thick, sticky mucus that can damage many of the body's organs.
Cystic Fibrosis (CF): Symptoms, Causes, Diagnosis, Treatment
Cystic fibrosis is caused by a change, or mutation, in a gene called CFTR (cystic fibrosis transmembrane conductance regulator). The protein in ...
Cystic fibrosis (CF) is a genetic condition affecting more than 11000 people in the UK. Find out more about the condition and how it is caused here.
Cystic Fibrosis - Symptoms and Causes - Penn Medicine
Cystic fibrosis (CF) is a disease that causes thick, sticky mucus to build up in the lungs, digestive tract, and other areas of the body.
Cystic Fibrosis (CF) | American Lung Association
Cystic fibrosis (CF) is an inherited disease that causes thickened mucus to form in the lungs, pancreas and other organs. In the lungs, this mucus blocks ...
Cystic fibrosis is an inherited condition in which the lungs and digestive system can become clogged with thick, sticky mucus.
Cystic Fibrosis: Practice Essentials, Background, Pathophysiology
Cystic fibrosis is a disease of exocrine gland function that involves multiple organ systems but chiefly results in chronic respiratory ...
Cystic fibrosis: Symptoms, treatments, causes, and diagnosis
CF is a genetic disorder linked to a mutation in the CFTR gene. This creates irregular proteins that cause mucus to become unusually thick and sticky.
Cystic Fibrosis (for Parents) | Nemours KidsHealth
What Are the Signs & Symptoms of Cystic Fibrosis? · lung infections or pneumonia · wheezing · coughing with thick mucus · bulky, greasy bowel movements ...
Learn About Cystic Fibrosis | American Lung Association
Key Facts · Cystic fibrosis (CF) is a life-threatening, genetic condition. · Both parents have to be carriers of an abnormal gene that gets passed on to their ...
Cystic Fibrosis Treatment, Symptoms, & Diagnosis | NORD
Cystic fibrosis is a genetic disorder that often affects multiple organ systems of the body. Cystic fibrosis is characterized by abnormalities affecting certain ...
Cystic fibrosis | About the Disease | GARD
Over time, mucus buildup and infections can lead to permanent lung damage, including the formation of scar tissue (fibrosis) and cysts in the lungs. CF is ...
Cystic Fibrosis Foundation
Non-profit organizationThe Cystic Fibrosis Foundation is a 501 non-profit organization in the United States established to provide the means to cure cystic fibrosis and ensure that those living with CF live long and productive lives.
Cystic fibrosis transmembrane conductance regulator
ProteinCystic fibrosis transmembrane conductance regulator is a membrane protein and anion channel in vertebrates that is encoded by the CFTR gene. Geneticist Lap-Chee Tsui and his team identified the CFTR gene in 1989 as the gene linked with CF.