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Cystic fibrosis

Cystic fibrosis (CF) is a genetic disorder which affects the cells that make mucus, sweat and the digestive fluids. In CF, these fluids become thick and eventually block respiratory and digestive passages. Increased mucus build-up in the airways cause breathing difficulty and can ultimately result in severe lung damage. Mucus can cause obstruction of the pancreatic ducts which may cause malabsorption of food. Obstruction of the bile ducts may result in severe liver cirrhosis. Thick secretions in the intestines may cause your feces to be very thick and cause constipation. CF is a severe condition that needs daily care. In India, about 3000 children are being born with cystic fibrosis every year.

Cystic fibrosis is caused due to the mutation in the CFTR gene (cystic fibrosis transmembrane conductance regular gene). For a child to acquire cystic fibrosis, both the parents must be carriers of the defective gene (CFTR gene).

Signs and symptoms



Cystic fibrosis is usually diagnosed at an early age. The signs and symptoms of cystic fibrosis are not the same for every child and they change over time. Some common symptoms of cystic fibrosis in a neonate are as follows:


Diagnosis of cystic fibrosis


If the physician suspects that a child may have cystic fibrosis, he may order for a newborn screening test for CF. If the child has a positive newborn screening, a sweat test is prescribed to confirm the diagnosis.


Prenatal Screening: CF can be diagnosed early by identifying the defective gene (CFTR gene) in the fetus.






Genetic tests for adults: Genetic tests for adults is usually suggested for couples before conceiving to help them find out either one or both are the carriers of the defective gene (CFTR gene).

Other tests: The following tests are done to monitor the organ function of in the patients with cystic fibrosis:



Treatment of cystic fibrosis


Treatment for the respiratory complications of CF:

Respiratory therapy aims at removing the mucus from the airways, improve breathing and improving lung function. This includes:


Treatment for the gastrointestinal complications of CF:

Digestive Enzyme Replacement Therapy: This therapy involves the use of drugs to aid the absorption of nutrients from food.

Nutrition therapy: In severe CF, nutritional supplements and foods rich in fats and calories need to be administered through a feeding tube.

Stool softeners: These help in relieving constipation.

Precautions


The following measures should be taken to prevent complications of CF


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We have the expertise of 34 + years in healthcare. Our labs are equipped with EQUAS (External Quality Assurance System) and loaded with full automated machines to ensure error free reports, with a quick turnaround time, and at an affordable price. For your convenience, we offer free home collection of samples.

For appointments, please call 9205478479.


References



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