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Mucoviscidosis (cystic Fibrosis) - Best Hospitals, Doctors, Prices - Booking Health

Treatment of Mucoviscidosis (cystic Fibrosis)

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Cost for Treatment of Mucoviscidosis (cystic Fibrosis)

The figures below show average prices for key services. Your final quote depends on the clinic, scope of diagnostics and length of stay.

Diagnosis of mucoviscidosis
5033.12
Diagnosis and conservative treatment of mucoviscidosis
4035.06
Pulmonary rehabilitation
0.00

Share a few details about your case and, within 24 hours, our medical team will send you a tailor‑made cost breakdown and the fastest treatment schedule — no hidden fees, no commitment, just clear numbers, and expert guidance for your specific situation.

Top Hospitals for Treatment of Mucoviscidosis (cystic Fibrosis)

Each hospital in this list meets Booking Health’s strict international standards: at least 250 surgeries per year, ISO‑certified quality management, and documented survival outcomes. Our medical board then ranks the clinics by clinical expertise, technology, and patient‑satisfaction scores.

According to the reputable Focus magazine, the Augustinerinnen Hospital Cologne ranks among the top medical facilities in North Rhine-Westphalia! The medical facility is an academic hospital of the University of Cologne, thanks to which it provides patients with highly effective treatment using the latest medical advances. The h
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According to Focus magazine, the University Hospital Heidelberg ranks among the top five hospitals in Germany! The hospital is one of the most advanced and reputable medical institutions not only in Germany, but throughout Europe. There are more than 43 specialized departments and 13 medical institutes, which cover all fields of
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According to the prestigious Focus magazine, the University Hospital RWTH Aachen ranks among the top German hospitals! As a maximum care university medical facility, the hospital guarantees patients first-class medical services combined with a respectful and human attitude. The hospital integrates all the modern options for the
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About the disease

Cystic fibrosis, also known as mucoviscidosis, is an inherited disorder that affects the lungs and digestive system by attacking the cells responsible for the production of bodily fluids. Mucus and saliva are thicker than normal, causing breathing passageways to become congested and the functioning of the lungs and pancreas to be disrupted. A child will only inherit cystic fibrosis if both parents have the defective gene that causes this disorder.

In the past, children with cystic fibrosis would often not live past their teens. Today, although it cannot be completely cured, this condition can be controlled and life expectancy has increased. People with cystic fibrosis can still go to school, attend university and go to work. Advancements in medicine mean that in the future, people with cystic fibrosis are expected to live a lot longer.

Babies are usually diagnosed with cystic fibrosis within the first few months after they are born. The diagnosis can be made even before any symptoms arise. In some cases, symptoms do not appear until adolescence or adulthood, but it is still important to attend regular check-ups at the doctor. Some people only experience symptoms of cystic fibrosis occasionally, while others suffer inflammation of the lungs or pancreas on a regular basis.

Symptoms

  • Cough with very thick mucus
  • Recurrent inflammation of lungs or pancreas
  • Shortness of breath
  • Wheezing
  • Frequent infections of respiratory and digestive systems
  • Constipation
  • Excessively salty sweat
  • Babies are slow to gain weight

Diagnosis

  • During a general examination, the doctor will use a stethoscope to listen to the child’s lungs, to check for wheezing or other breathing problems.
  • The doctor will also ask the child’s parents if they or anyone in the family have cystic fibrosis.
  • A blood test can be used to analyze the chemicals released by the child’s pancreas. High levels of one specific chemical can indicate the presence of cystic fibrosis.
  • Genetic testing can establish whether a child has a gene that causes cystic fibrosis.

Treatment

  • Conservative treatment can alleviate the symptoms of cystic fibrosis and prolong life expectancy.
  • Various antibiotics and anti-inflammatory drugs are prescribed, to prevent the reappearance of infections and reduce inflammation.
  • Special drugs that thin the mucus are also prescribed, to improve the functioning of the lungs.

Authors: Dr. Vadim ZhiliukDr. Sergey Pashchenko

To check for the Mucoviscidosis (cystic fibrosis) you can submit a request on BookingHealth and our managers will find the best hospital that is specialized in Mucoviscidosis (cystic fibrosis) to fulfill your needs
Cost of Mucoviscidosis (cystic fibrosis) treatment varies from 4035.06 to 18489.75
The best hospitals for Mucoviscidosis (cystic fibrosis) treatment are: Augustinerinnen Hospital Cologne, University Hospital Heidelberg, University Hospital RWTH Aachen

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  • Analysis of statistics and selection of the best clinic
  • Fixed final price (additional costs will be covered by insurance)
  • One year of medical support by your attending physician after the treatment

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Motivator

Booking Health guarantees

  • Analysis of statistics and selection of the best clinic
  • Fixed final price (additional costs will be covered by insurance)
  • One year of medical support by your attending physician after the treatment