Stanford CF Education Day DVD Order Form Version 2 pub - cfri 2025

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Cystic fibrosis can be diagnosed at any age, but it is most commonly diagnosed in infants and young children. In fact, about 70% of people with cystic fibrosis are diagnosed before the age of two. The disease can also be diagnosed in adults, but this is less common.
CF causes thick mucus that clogs certain organs, such as the lungs, pancreas, and intestines. This may cause malnutrition, poor growth, frequent respiratory infections, breathing problems, and chronic lung disease.
For people with CF, being close to others with the disease puts them at greater risk of getting and spreading dangerous germs and bacteria. This is called cross‐infection. Not only are these dangerous germs difficult to treat, but they can also lead to worsening symptoms and faster decline in lung function.
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Beware: there are other diseases that can mimic cystic fibrosis: Hirschsprungs disease. bronchiolitis. protein calorie malnutrition. celiac disease. giardiasis. asthma. immunodeficiency. biliary atresia.
However, not every case of CF presents with meconium ileus in the newborn, failure to thrive, or severe lung disease. Atypical CF is characterized by a milder form of the disease usually remaining undiagnosed for years, even into late adulthood [2].
Symptoms for Cystic Fibrosis in Adults A persistent cough. Wheezing. Lung infections. Pancreatitis (inflammation of the pancreas) Sinusitis. Malnutrition. Infertility. Arthritis.
Cystic Fibrosis Symptoms Trouble with bowel movements or frequent, greasy stools. Wheezing or trouble breathing. Frequent lung infections. Infertility, especially in men. Trouble growing or gaining weight. Skin that tastes very salty.
Cystic fibrosis is caused by a faulty gene that a child inherits from both of their parents. The faulty gene means that some cells struggle to move salt and water across the cell wall. This, along with recurrent infections, can result in a build-up of thick, sticky mucus in the bodys tubes and passageways.