Short Description

NGS genetic DNA test detecets for variant and mutation detection in SLC26A6 gene for Hyperoxaluria, SLC26A6 related

PreTest Information

Clinical History of Patient who is going for SLC26A6 Gene Hyperoxaluria, SLC26A6 related NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Hyperoxaluria, SLC26A6 related

Detail Description

SLC26A6 Gene Hyperoxaluria: Symptoms, Diagnosis, and NGS Genetic DNA Test Cost in India

Hyperoxaluria is a rare genetic disorder that causes the overproduction of oxalate, a compound that can form kidney stones and cause damage to other organs. SLC26A6 gene hyperoxaluria is a specific type of hyperoxaluria that is caused by mutations in the SLC26A6 gene. This gene is responsible for the transport of oxalate in the body, and mutations can lead to the accumulation of oxalate in the urine and other tissues.

Some of the symptoms of SLC26A6 gene hyperoxaluria include:

• Kidney stones
• Chronic kidney disease
• Calcium oxalate deposits in other organs, such as the eyes, skin, and heart
• Abdominal pain
• Blood in the urine
• Frequent urination
• Urinary tract infections

If you are experiencing any of these symptoms, it is important to see a doctor for a proper diagnosis. SLC26A6 gene hyperoxaluria can be diagnosed through genetic testing, which looks for mutations in the SLC26A6 gene. This testing can be done through NGS (next-generation sequencing) genetic DNA testing.

NGS genetic DNA testing is a type of genetic testing that uses advanced sequencing technology to analyze a person's DNA. This technology allows for the analysis of multiple genes at once, making it a powerful tool for genetic diagnosis. The cost of NGS genetic DNA testing for SLC26A6 gene hyperoxaluria in India is typically around INR 20,000.

It is important to note that genetic testing for SLC26A6 gene hyperoxaluria is not typically covered by insurance, so patients should be prepared to pay out of pocket for this testing.

Overall, SLC26A6 gene hyperoxaluria is a rare genetic disorder that can have serious health consequences if left untreated. If you are experiencing symptoms of this condition, it is important to see a doctor for a proper diagnosis. NGS genetic DNA testing can be a useful tool in the diagnosis of this condition, but patients should be prepared to pay for this testing out of pocket.

If you are interested in learning more about SLC26A6 gene hyperoxaluria or NGS genetic DNA testing, contact DNA Labs India for more information.

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 SLC26A6 Gene Hyperoxaluria, SLC26A6 related NGS Genetic DNA Test