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Cystic fibrosis - Symptoms and causes - Mayo Clinic
https://www.mayoclinic.org/diseases-conditions/cystic-fibrosis/symptoms-causes/syc-20353700
Web ResultNov 23, 2021 · Cystic fibrosis (CF) is an inherited disorder that causes severe damage to the lungs, digestive system and other organs in the body. Cystic fibrosis affects the cells that produce mucus, sweat and digestive juices. These secreted fluids are normally thin and slippery.
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Cystic Fibrosis (CF): Causes, Symptoms, Diagnosis & Treatment
https://my.clevelandclinic.org/health/diseases/9358-cystic-fibrosis
Web ResultOct 8, 2021 · Cystic fibrosis (CF) is a genetic (inherited) disease that causes sticky, thick mucus to build up in organs, including the lungs and the pancreas. In people who have CF, thick mucus clogs the airways and makes it difficult to breathe. Management includes ways of clearing lungs and eating correctly.
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Cystic Fibrosis | Johns Hopkins Medicine
https://www.hopkinsmedicine.org/health/conditions-and-diseases/cystic-fibrosis
Web ResultCystic fibrosis (CF) is an inherited life-threatening disease that affects many organs. It causes changes in the electrolyte transport system. People with CF have problems in the glands that produce sweat and mucus. CF causes thick mucus that clogs certain organs such as the lungs, pancreas, and intestines.
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Cystic Fibrosis - What Is Cystic Fibrosis? | NHLBI, NIH
https://www.nhlbi.nih.gov/health/cystic-fibrosis
Web ResultNov 21, 2023 · Causes. Last updated on November 21, 2023. Cystic fibrosis is a life-shortening inherited condition that affects a certain protein called CFTR in the body. The faulty CFTR protein causes problems with the body’s cells, tissues, and organs and the glands that make mucus and sweat.
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Cystic fibrosis - Wikipedia, the free encyclopedia
https://en.wikipedia.org/wiki/Cystic_fibrosis
Web ResultCystic fibrosis (also known as CF or mucoviscidosis) is an autosomal recessive genetic disorder affecting most critically the lungs, and also the pancreas, liver, and intestine.
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The Basics of CF | The Cystic Fibrosis Center at Stanford
https://med.stanford.edu/cfcenter/education/english/BasicsOfCF.html
Web ResultWhat Is CF? Cystic Fibrosis (CF) is one of the most common genetic (inherited) diseases in America. It is also one of the most serious. It mainly affects the lungs and the digestive systems in the body, causing breathing problems and problems digesting foods. It is a chronic disease that currently has no cure. What Happens?
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Cystic fibrosis pathophysiology (video) | Khan Academy
https://www.khanacademy.org/science/health-and-medicine/respiratory-system-diseases/cystic-fibrosis/v/cystic-fibrosis-pathophysiology
Web ResultThe pathophysiology of CF is more about the accumulation of thick mucus in the lungs (problems with breathing, the blood does not have enough oxygen), the digestive tract (malabsoption of nutriments, it's very serious for children because they can't grow!) . This results in frequent infections.
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About Cystic Fibrosis | Cystic Fibrosis Foundation
https://www.cff.org/intro-cf/about-cystic-fibrosis
Web ResultSymptoms of CF. People with CF can have a variety of symptoms, including: Very salty-tasting skin. Persistent coughing, at times with phlegm. Frequent lung infections including pneumonia or bronchitis. Wheezing or shortness of breath. Poor growth or weight gain in spite of a good appetite.
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Cystic fibrosis: Clinical manifestations and diagnosis - UpToDate
https://www.uptodate.com/contents/cystic-fibrosis-clinical-manifestations-and-diagnosis
Web ResultMar 7, 2023 · INTRODUCTION. Cystic fibrosis (CF) is a multisystem disorder caused by pathogenic mutations of the CFTR gene (CF transmembrane conductance regulator). Typical symptoms and signs include persistent pulmonary infection, pancreatic insufficiency, and elevated sweat chloride levels.
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Cystic Fibrosis: an Update on Disease Pathophysiology ... - Springer
https://link.springer.com/article/10.1007/s40521-019-00211-4
Web ResultJul 2, 2019 · To explain the underlying pathophysiology of cystic fibrosis and to describe current treatment modalities for disease manifestations, including an introduction to novel therapies known as CFTR modulator drugs, which are now available to over 50% of people with cystic fibrosis. Recent findings.
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