Cystic fibrosis
volume
British pronunciation/sˈɪstɪk fɪbɹˈəʊsɪs/
American pronunciation/sˈɪstɪk fɪbɹˈoʊsɪs/

Definizione e Significato di "cystic fibrosis"

Cystic fibrosis
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fibrosi cistica

a genetic disorder causing the production of thick and sticky mucus, affecting the respiratory and digestive systems and leading to various complications

What is "cystic fibrosis"?

Cystic fibrosis is a genetic disorder that affects the lungs and digestive system. It is caused by mutations in the CFTR gene, which leads to the production of thick, sticky mucus that can clog the airways and blocks the pancreas, the organ located behind the stomach that produces enzymes to help digest food and hormones. Symptoms of cystic fibrosis vary but often include persistent coughing, frequent lung infections, difficulty breathing, poor growth, and digestive problems such as difficulty digesting food and absorbing nutrients. Cystic fibrosis is a lifelong condition that requires ongoing medical care. Treatment typically involves medications to thin mucus, prevent infections, improve lung function, and support digestion, as well as therapies and exercise to help clear mucus from the lungs.

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Individuals with cystic fibrosis often experience chronic lung infections due to the difficulty in clearing mucus from the airways.
Support from healthcare teams is essential for individuals with cystic fibrosis.
Cystic fibrosis is a lifelong condition, and management aims to alleviate symptoms and improve quality of life.
Advances in research have led to the development of targeted therapies addressing specific genetic mutations in cystic fibrosis.
Individuals with cystic fibrosis are at risk of developing complications such as diabetes and liver disease.
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