Short Description

NGS genetic DNA test detecets for variant and mutation detection in SFTPA1 gene for Pulmonary fibrosis, idiopathic

PreTest Information

Clinical History of Patient who is going for SFTPA1 Gene Pulmonary fibrosis, idiopathic NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SFTPA1 Gene Pulmonary fibrosis, idiopathic NGS Genetic DNA Test gene SFTPA1

Detail Description

SFTPA1 Gene and Pulmonary Fibrosis: Symptoms, Diagnosis, and NGS Genetic DNA Test Cost in India

Pulmonary fibrosis is a condition that affects the lungs and causes scarring, which makes it difficult for the lungs to function properly. Idiopathic pulmonary fibrosis (IPF) is a type of pulmonary fibrosis that has no known cause. However, recent studies have shown that genetics play a significant role in IPF development, specifically the SFTPA1 gene.

What is the SFTPA1 Gene?

The SFTPA1 gene is responsible for producing surfactant protein A (SP-A), which is a protein that helps keep the lungs clear of debris and infections. Mutations in the SFTPA1 gene have been linked to the development of pulmonary fibrosis, including IPF. Researchers believe that these mutations cause SP-A to function improperly, leading to the development of scarring in the lungs.

Symptoms of Pulmonary Fibrosis

The symptoms of pulmonary fibrosis can vary from person to person, but some common symptoms include:

• Shortness of breath
• Dry, persistent cough
• Fatigue
• Weakness
• Chest discomfort or pain

If you are experiencing any of these symptoms, it is important to talk to your doctor, as early diagnosis and treatment can improve outcomes.

Diagnosis of Pulmonary Fibrosis

Diagnosing pulmonary fibrosis can be challenging, as the symptoms can be similar to those of other lung conditions. However, there are several tests that can help diagnose the condition, including:

• Chest X-ray
• High-resolution computed tomography (HRCT) scan
• Pulmonary function tests (PFTs)
• Lung biopsy

If your doctor suspects that you have pulmonary fibrosis, they may recommend one or more of these tests to confirm the diagnosis.

NGS Genetic DNA Test for SFTPA1 Gene Mutations

If you have been diagnosed with IPF or have a family history of the condition, your doctor may recommend genetic testing to determine if you have mutations in the SFTPA1 gene. Next-generation sequencing (NGS) is a type of genetic testing that can analyze multiple genes at once, making it a faster and more cost-effective way to identify genetic mutations.

NGS Genetic DNA Test Cost in India

The cost of NGS genetic DNA testing for SFTPA1 gene mutations in India can vary depending on the laboratory and the specific test being performed. However, on average, the cost for this type of testing is around INR 20,000. It is important to note that this cost may or may not be covered by insurance, so it is important to check with your provider before undergoing testing.

Conclusion

If you or a loved one is experiencing symptoms of pulmonary fibrosis or has been diagnosed with IPF, it is important to talk to your doctor about genetic testing for SFTPA1 gene mutations. Early diagnosis and treatment can improve outcomes and quality of life, and NGS genetic DNA testing can help identify genetic mutations more quickly and cost-effectively than traditional genetic testing methods.

At DNA Labs India, we offer NGS genetic DNA testing services for SFTPA1 gene mutations and other genetic conditions. Contact us today to learn more about our testing services and how we can help you and your family.