Short Description

NGS genetic DNA test detecets for variant and mutation detection in SLC9A3R1 gene for Nephrolithiasis/osteoporosis, hypophosphatemic, type 2

PreTest Information

Clinical History of Patient who is going for SLC9A3R1 Gene Nephrolithiasis/osteoporosis, hypophosphatemic, type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC9A3R1 Gene Nephrolithiasis/osteoporosis, hypophosphatemic, type 2 NGS Genetic DNA Test gene SLC9A3R1

Detail Description

SLC9A3R1 Gene Nephrolithiasis/Osteoporosis, Hypophosphatemic, Type 2 NGS Genetic DNA Test Cost INR:20000 Symptoms Diagnosis

Have you been experiencing symptoms of nephrolithiasis or osteoporosis? Are you concerned about hypophosphatemic type 2? The SLC9A3R1 gene is a key player in the development of these conditions, and genetic testing can provide valuable insights into your risk.

What is the SLC9A3R1 Gene?

The SLC9A3R1 gene is responsible for producing a protein called NHE3, which plays an important role in the kidneys' ability to regulate the levels of phosphate in the body. When this gene is mutated or damaged, it can lead to a condition called hypophosphatemic type 2, which is characterized by low levels of phosphate in the blood.

Low levels of phosphate can lead to a variety of health problems, including nephrolithiasis (kidney stones) and osteoporosis (weak and brittle bones).

What are the Symptoms of Hypophosphatemic Type 2?

Symptoms of hypophosphatemic type 2 can vary widely, but may include:

• Weak and brittle bones
• Delayed growth and development in children
• Muscle weakness and pain
• Loss of appetite
• Fatigue

If you are experiencing any of these symptoms, it is important to speak with your doctor to determine the underlying cause and the best course of treatment.

Diagnosing Hypophosphatemic Type 2

Diagnosing hypophosphatemic type 2 typically involves a combination of physical exams, blood tests, and genetic testing.

A blood test can measure the levels of phosphate in your blood, while genetic testing can identify mutations in the SLC9A3R1 gene that may be contributing to your symptoms.

The Benefits of Genetic Testing

Genetic testing can provide valuable insights into your risk for a variety of health conditions, including hypophosphatemic type 2, nephrolithiasis, and osteoporosis.

By identifying mutations in the SLC9A3R1 gene, genetic testing can help doctors determine the underlying cause of your symptoms and develop a personalized treatment plan that is tailored to your unique needs.

The Cost of NGS Genetic DNA Testing

The cost of NGS genetic DNA testing for the SLC9A3R1 gene is INR:20000. While this may seem expensive, the benefits of genetic testing can far outweigh the cost.

By identifying the underlying cause of your symptoms, genetic testing can help you avoid unnecessary treatments and procedures, as well as provide valuable insights into your risk for future health problems.

Conclusion

If you are experiencing symptoms of hypophosphatemic type 2, nephrolithiasis, or osteoporosis, genetic testing may be a valuable tool in your diagnosis and treatment plan.

Speak with your doctor today to learn more about the benefits of genetic testing and whether it is right for you.

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 SLC9A3R1 Gene Nephrolithiasis/osteoporosis, hypophosphatemic, type 2 NGS Genetic DNA Test