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  • Cystic fibrosis - Symptoms and causes - Mayo Clinic
    Cystic fibrosis is a disorder that damages your lungs, digestive tract and other organs It's an inherited disease caused by a defective gene that can be passed from generation to generation Cystic fibrosis affects the cells that produce mucus, sweat and digestive juices
  • Cystic fibrosis - Diagnosis and treatment - Mayo Clinic
    Take time to learn about cystic fibrosis If your child has cystic fibrosis, encourage your child to learn about CF Find out how medical care is managed for children with CF as they grow older and reach adulthood
  • Fibrosis quística - Síntomas y causas - Mayo Clinic
    Si tú o tu hijo tienen síntomas de fibrosis quística (o si alguien de tu familia tiene fibrosis quística) habla con tu profesional de atención médica sobre la posibilidad de realizar pruebas para detectar la afección
  • What is cystic fibrosis? A Mayo Clinic expert explains
    Cystic fibrosis is a disorder that damages your lungs, digestive tract and other organs It's an inherited disease caused by a defective gene that can be passed from generation to generation Cystic fibrosis affects the cells that produce mucus, sweat and digestive juices
  • Cystic fibrosis care at Mayo Clinic
    Experts at Mayo Clinic's campuses in Minnesota and Florida offer the latest in diagnosis and treatment of cystic fibrosis A trained, multispecialty team of experienced doctors and other medical professionals evaluate and treat people who have CF
  • A new future for cystic fibrosis - Mayo Clinic
    Cystic fibrosis is one of the most common genetically transmitted diseases It affects about 30,000 people in the United States Double-lung transplant can extend and improve quality of life for people with cystic fibrosis
  • Mayo Clinics Cystic Fibrosis Foundation-designated CF care center
    Cystic fibrosis (CF) is a multisystem disorder that remains the most common genetic disease of Caucasians The clinical manifestations leading to chronic lung disease and malnutrition are a direct result of mutation of the CF transmembrane conductance regulator (CFTR) protein, which is expressed predominantly in epithelial cells





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