Short Description

NGS genetic DNA test detecets for variant and mutation detection in INF2 gene for Focal segmental glomerulosclerosis type 5

PreTest Information

Clinical History of Patient who is going for INF2 Gene Focal segmental glomerulosclerosis type 5 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with INF2 Gene Focal segmental glomerulosclerosis type 5 NGS Genetic DNA Test gene INF2

Detail Description

INF2 Gene Focal Segmental Glomerulosclerosis Type 5 NGS Genetic DNA Test Cost INR:20000 Symptoms Diagnosis

Focal segmental glomerulosclerosis (FSGS) is a rare kidney disorder that affects the filtering units of the kidneys called glomeruli. It is a serious condition that can lead to kidney failure. FSGS can be caused by genetic mutations, and one of the genes associated with FSGS is the INF2 gene.

The INF2 gene provides instructions for making a protein that is involved in the organization and movement of the cell's internal scaffolding, or cytoskeleton. Mutations in the INF2 gene can lead to abnormal cytoskeleton formation, which can cause kidney damage and FSGS.

The NGS Genetic DNA Test is a genetic test that can detect mutations in the INF2 gene associated with FSGS. The test uses Next-Generation Sequencing (NGS) technology, which is a high-throughput DNA sequencing method that can sequence millions of DNA fragments simultaneously. This allows for the detection of mutations in the INF2 gene with high accuracy.

Symptoms of FSGS

The symptoms of FSGS can vary widely and may include:

• Proteinuria (excess protein in the urine)
• Edema (swelling) in the legs, feet, and ankles
• High blood pressure
• Fatigue
• Loss of appetite
• Nausea and vomiting

If you are experiencing any of these symptoms, it is important to see a doctor for an accurate diagnosis.

Diagnosis of FSGS

Diagnosis of FSGS usually involves a combination of tests, including:

• Urine tests to check for proteinuria
• Blood tests to check kidney function and electrolyte levels
• Imaging tests, such as an ultrasound or CT scan, to look for abnormalities in the kidneys
• Kidney biopsy, which involves taking a small sample of kidney tissue to examine under a microscope

If FSGS is diagnosed, genetic testing may be recommended to determine if a genetic mutation, such as one in the INF2 gene, is the cause of the condition.

Cost of INF2 Gene FSGS Type 5 NGS Genetic DNA Test

The cost of the INF2 Gene FSGS Type 5 NGS Genetic DNA Test in India is typically around INR 20,000. However, prices may vary depending on the laboratory or clinic where the test is performed.

Conclusion

FSGS is a serious kidney disorder that can be caused by genetic mutations, such as those in the INF2 gene. The NGS Genetic DNA Test is a genetic test that can detect mutations in the INF2 gene associated with FSGS. If you are experiencing symptoms of FSGS, it is important to see a doctor for an accurate diagnosis and to discuss whether genetic testing is appropriate for you.

If you are interested in getting the INF2 Gene FSGS Type 5 NGS Genetic DNA Test, be sure to do your research and find a reputable laboratory or clinic that offers the test at a reasonable cost.

Remember, early detection and treatment can make a big difference in the management of FSGS and can help prevent kidney failure.

For more information on FSGS and genetic testing, contact DNA Labs India today.

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 INF2 Gene Focal segmental glomerulosclerosis type 5 NGS Genetic DNA Test