Short Description

NGS genetic DNA test detecets for variant and mutation detection in SCNN1A gene for Bronchiectasis with or without elevated sweat chloride type 2

PreTest Information

Clinical History of Patient who is going for SCNN1A Gene Bronchiectasis with or without elevated sweat chloride type 2 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Bronchiectasis with or without elevated sweat chloride type 2

Detail Description

SCNN1A Gene Bronchiectasis: Symptoms, Diagnosis, and Genetic Testing Cost

Bronchiectasis is a lung disease that causes the bronchial tubes to widen and become inflamed. This condition can lead to chronic infections, coughing, and difficulty breathing. While bronchiectasis can be caused by a variety of factors, including infections and autoimmune disorders, some cases are caused by genetic mutations.

One such mutation is found in the SCNN1A gene, which is responsible for producing a protein that regulates the movement of salt and water in the lungs. When this gene is mutated, it can cause a type of bronchiectasis that is associated with elevated sweat chloride levels.

Symptoms of SCNN1A Gene Bronchiectasis

The symptoms of SCNN1A gene bronchiectasis are similar to those of other types of bronchiectasis. They may include:

• Chronic coughing
• Shortness of breath
• Wheezing
• Chest pain
• Frequent lung infections

Diagnosing SCNN1A Gene Bronchiectasis

Diagnosing SCNN1A gene bronchiectasis typically involves a combination of medical history, physical examination, and diagnostic tests. Your doctor may ask you about your symptoms, family history, and any environmental factors that may be contributing to your condition.

Diagnostic tests may include:

• Chest X-ray or CT scan
• Sputum culture to test for bacteria
• Pulmonary function test to measure lung function
• Sweat chloride test to measure salt levels in your sweat
• Genetic testing to identify mutations in the SCNN1A gene

NGS Genetic DNA Test Cost for SCNN1A Gene Bronchiectasis

The cost of genetic testing for SCNN1A gene bronchiectasis varies depending on the type of test you need and where you live. In India, you can expect to pay around INR 20,000 for a next-generation sequencing (NGS) DNA test that looks for mutations in the SCNN1A gene.

While this may seem like a significant expense, genetic testing can provide important information about your condition that can help guide your treatment and management. It can also help identify other family members who may be at risk for the same condition.

Conclusion

SCNN1A gene bronchiectasis is a type of lung disease that is caused by mutations in the SCNN1A gene. Symptoms may include chronic coughing, shortness of breath, and frequent lung infections. Diagnosis typically involves a combination of medical history, physical examination, and diagnostic tests, including genetic testing. The cost of NGS genetic DNA testing for SCNN1A gene bronchiectasis in India is around INR 20,000. If you are experiencing symptoms of bronchiectasis or have a family history of the condition, talk to your doctor about whether genetic testing may be appropriate for you.

Remember to seek medical attention for any respiratory issues you may be experiencing. Stay healthy and take care!

Before getting tested ask for Raw Data, FASTQ, and VCF files along with clinical test report from DNA Testing Lab. DNA Labs India is the Only lab that is transparent and will share Raw Data, FASTQ, and VCF files along with the conclusive clinical report for SCNN1A Gene Bronchiectasis with or without elevated sweat chloride type 2 NGS Genetic DNA Test