Short Description

NGS genetic DNA test detecets for variant and mutation detection in EGFR gene for Nonsmall cell lung cancer, familial, susceptibility to

PreTest Information

Clinical History of Patient who is going for EGFR Gene Nonsmall cell lung cancer, familial, susceptibility to NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with EGFR Gene Nonsmall cell lung cancer, familial, susceptibility to NGS Genetic DNA Test gene EGFR

Detail Description

EGFR Gene and Nonsmall Cell Lung Cancer: Susceptibility and Diagnosis through NGS Genetic DNA Test

Lung cancer is one of the leading causes of cancer-related deaths worldwide. Among the different types of lung cancer, non-small cell lung cancer (NSCLC) is the most common, accounting for around 85% of all cases. NSCLC can be caused by various genetic mutations, and one of the most significant mutations is in the EGFR gene. Genetic testing for EGFR mutations can provide valuable information for the diagnosis and treatment of NSCLC, especially in cases of familial susceptibility. In this blog, we will discuss the importance of EGFR gene testing for NSCLC, its symptoms, diagnosis, and the cost of NGS Genetic DNA Test in India.

The Role of EGFR Gene in NSCLC

EGFR (epidermal growth factor receptor) is a protein that plays a crucial role in the growth and survival of cells. Mutations in the EGFR gene can cause the protein to become overactive, leading to uncontrolled cell growth and division, which can result in cancer. EGFR mutations are commonly found in NSCLC, and they are more prevalent in certain populations, such as Asians and non-smokers.

Symptoms of NSCLC

The symptoms of NSCLC can vary depending on the stage and location of the cancer. Some common symptoms include:

• Coughing up blood
• Chest pain
• Shortness of breath
• Wheezing
• Hoarseness
• Weight loss

It is important to note that these symptoms can also be caused by other conditions, so it is essential to seek medical attention if you experience any of these symptoms.

Diagnosis of NSCLC

The diagnosis of NSCLC involves various tests and procedures, including:

• Physical examination and medical history
• Chest X-ray or CT scan
• Sputum cytology
• Biopsy

If NSCLC is suspected, a biopsy is typically performed to obtain a tissue sample for further testing. The tissue sample can be tested for EGFR mutations, which can help guide treatment decisions.

NGS Genetic DNA Test Cost in India

Next-generation sequencing (NGS) is a powerful technology that can sequence large amounts of DNA rapidly and accurately. NGS can be used to detect EGFR mutations in NSCLC, which can provide valuable information for the diagnosis and treatment of the disease.

The cost of NGS Genetic DNA Test for EGFR mutations in India can vary depending on the laboratory and the specific test being performed. On average, the cost of the test can range from INR 15,000 to INR 25,000. However, it is essential to note that the cost of the test should not be the only consideration when choosing a laboratory for genetic testing. The quality and accuracy of the test results are equally important.

Conclusion

EGFR gene testing can provide valuable information for the diagnosis and treatment of NSCLC, especially in cases of familial susceptibility. Symptoms of NSCLC can vary, and it is essential to seek medical attention if any symptoms are experienced. The diagnosis of NSCLC involves various tests and procedures, including biopsy for EGFR mutation testing. The cost of NGS Genetic DNA Test for EGFR mutations in India can range from INR 15,000 to INR 25,000. However, the quality and accuracy of the test results should be the primary consideration when choosing a laboratory for genetic testing.

At DNA Labs India, we offer high-quality and accurate genetic testing services, including EGFR mutation testing for NSCLC. Our NGS Genetic DNA Test is performed by experienced professionals using state-of-the-art equipment and technology. Contact us today to learn more about our genetic testing services.