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

SLC9A3R1 gene is associated with the development of nephrolithiasis/osteoporosis, hypophosphatemic, type 2. This condition is characterized by the formation of kidney stones and weak bones due to low levels of phosphorus in the blood. The SLC9A3R1 gene provides instructions for making a protein that is involved in the absorption of phosphate from the digestive tract. Mutations in this gene can lead to a decrease in the absorption of phosphate, which can cause hypophosphatemia, a condition characterized by low levels of phosphorus in the blood.

Symptoms of Nephrolithiasis/Osteoporosis, Hypophosphatemic, Type 2

The symptoms of nephrolithiasis/osteoporosis, hypophosphatemic, type 2 include:

• Kidney stones
• Weakened bones
• Muscle weakness
• Joint pain
• Short stature
• Dental problems

Diagnosis of Nephrolithiasis/Osteoporosis, Hypophosphatemic, Type 2

The diagnosis of nephrolithiasis/osteoporosis, hypophosphatemic, type 2 is based on the symptoms and the results of genetic testing. A blood test can be used to measure the levels of phosphorus in the blood. Imaging tests, such as X-rays and CT scans, can be used to detect kidney stones and bone density.

NGS Genetic DNA Test for SLC9A3R1 Gene Nephrolithiasis/Osteoporosis, Hypophosphatemic, Type 2

The NGS Genetic DNA Test for SLC9A3R1 Gene Nephrolithiasis/Osteoporosis, Hypophosphatemic, Type 2 is a genetic test that can detect mutations in the SLC9A3R1 gene. This test can help diagnose the condition and identify carriers of the gene mutation. The test is done using a blood or saliva sample and the results are usually available in a few weeks.

Cost of NGS Genetic DNA Test for SLC9A3R1 Gene Nephrolithiasis/Osteoporosis, Hypophosphatemic, Type 2

The cost of the NGS Genetic DNA Test for SLC9A3R1 Gene Nephrolithiasis/Osteoporosis, Hypophosphatemic, Type 2 in India is around INR 20,000.

Conclusion

The NGS Genetic DNA Test for SLC9A3R1 Gene Nephrolithiasis/Osteoporosis, Hypophosphatemic, Type 2 is a useful tool in the diagnosis and management of this condition. It can help identify carriers of the gene mutation and provide information on the risk of passing it on to future generations. If you suspect you or a family member may have this condition, it is important to talk to a healthcare professional and consider genetic testing.

At DNA Labs India, we offer a wide range of genetic testing services, including the NGS Genetic DNA Test for SLC9A3R1 Gene Nephrolithiasis/Osteoporosis, Hypophosphatemic, Type 2. Our team of experts is dedicated to providing accurate and reliable results to help you make informed healthcare decisions. Contact us today to learn more about our services.

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