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Cystic Fibrosis


Research Notes on Cystic Fibrosis

Cystic fibrosis (also known as CF, mucoviscoidosis, or mucoviscidosis) is a hereditary disease that affects the exocrine (mucus) glands of the lungs, liver, pancreas, and intestines, causing progressive disability due to multisystem failure. Thick mucus production, as well as a less competent immune system, results in frequent lung infections. Diminished secretion of pancreatic enzymes is the main cause of poor growth, fatty diarrhea and deficiency in fat-soluble vitamins. Males can be infertile due to the condition congenital bilateral absence of the vas deferens. Often, symptoms of CF appear in infancy and childhood. ...read more from Wikipedia

Fast Facts:

  • Cystic fibrosis can be diagnosed before birth with genetic testing.
  • There is no cure for cystic fibrosis, however treatment of airway function improves the quality of life.
  • Most people with cystic fibrosis die young in their 20's and 30's due to lung failure.

5 Great Resources on Cystic Fibrosis

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5 Latest Headlines on Cystic Fibrosis

What is Cystic Fibrosis?

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What Are The Causes and Complications of Cystic Fibrosis?

What Are The Treatments and Medications for Cystic Fibrosis?

What Are Statistics and Survival Rates of Cystic Fibrosis?

Wisdom, Personal Experiences and Blogs about Cystic Fibrosis

Foundations and Support Groups on Cystic Fibrosis

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Scientific and Medical Journal Articles on Cystic Fibrosis

Clinical Trials on Cystic Fibrosis

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