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Cystic Fibrosis, a chronic genetic disease, is caused by a faulty protein that affects the body's cells, tissues, and glands responsible for producing mucus and sweat. The mucus protects the airways, digestive tract, and other organs and tissues. In people with cystic fibrosis, the mucus becomes thick and sticky, making it difficult for the body to clear it out. While CF can’t be cured completely, our Paediatric Pulmonologists and Sleep Medicine Specialists at Cystic Fibrosis Clinic, Manipal Hospitals can help you control the disease and live a normal life with effective diagnostics and management. Consult our specialists in Bangalore if you need cystic fibrosis treatment
The Cystic Fibrosis Clinic at Manipal Hospitals Bangalore focuses on providing high-quality, specialized care for children with Cystic Fibrosis (CF), and their families. CF is a chronic disease that needs regular follow-up even if the child has no symptoms.
Our team includes experts from the fields of Paediatric Pulmonology, Paediatric Gastroenterology, Paediatric Endocrinology, ENT, Clinical Genetics, Physiotherapy, and Nutrition at Manipal Hospitals with a collective aim to provide a holistic management approach for children suffering from CF. Dr. Kavita Kotha, a Paediatric Pulmonologist from Nationwide Children’s Hospital Columbus, Ohio, USA will also be a part of our multidisciplinary team, providing valuable guidance. Consult our specialists in Bangalore if you need fibrosis treatment.
Cystic Fibrosis is a chronic genetic disorder that damages the lungs and digestive system by affecting the protein in the body. It affects the body's cells, tissues, and glands that produce mucus and sweat. Naturally produced mucus, an important substance, is slippery and protects the airways, digestive tract, and other organs and tissues. But, the mucus becomes thick and sticky in people with cystic fibrosis which makes it difficult for the body to clear it out. This can lead to serious health issues like lung disease, liver disease, and diabetes over time.
CF is more common among the younger population (below 18 years) with 75% of patients being diagnosed with the condition within 2 years of age. Patients need regular follow-up even if the child has no symptoms. Managing CF requires a multidisciplinary approach. Early identification of problems leads to more effective management and better outcomes.
Persistent cough, sometimes with watery content (mucus/phlegm) or blood
Wheezing
Shortness of breath
Salty sweating
Frequent lung infections - Pneumonia or Bronchitis.
Poor growth or weight gain despite a good appetite
Changes in bowel movements - Constipation or Diarrhoea
Bulky, greasy stools
At present, there is no cure for cystic fibrosis, but medical and psychosocial support has made it possible for young children and teenagers to control the disease and lead a normal, productive life. The management of CF aims to relieve the symptoms and slow the progress of the disease.
At our monthly Cystic Fibrosis Clinic, our Paediatric Pulmonologists will provide valuable guidance based on a thorough evaluation and tests. Therapies for CF include:
Chest physical therapy to clear excess mucus from the lungs.
Medications – bronchodilators, anti-inflammatory medications, and antibiotics to reduce mucus, improve breathing, and treat infections.
Management of digestive problems associated with CF with proper diet regime and supplements.
Regular screening for complications like early-stage liver disease and diabetes.
Psychosocial support to help the child manage isolation and mental health issues if occur.
