Short Description

NGS genetic DNA test detecets for variant and mutation detection in CLCNKB gene for Bartter syndrome type 3

PreTest Information

Clinical History of Patient who is going for CLCNKB Gene Bartter syndrome type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CLCNKB Gene Bartter syndrome type 3 NGS Genetic DNA Test gene CLCNKB

Detail Description

CLCNKB Gene Bartter Syndrome Type 3 NGS Genetic DNA Test Cost INR 20000: Symptoms and Diagnosis

Bartter syndrome is a rare genetic disorder that affects the kidneys' ability to reabsorb salt and water from the urine. This results in excessive salt and water loss in the urine and leads to electrolyte imbalances. There are several types of Bartter syndrome, and type 3 is caused by mutations in the CLCNKB gene.

NGS (Next-Generation Sequencing) genetic DNA testing is a powerful tool used to detect genetic mutations that cause diseases like Bartter syndrome. DNA Labs India offers a CLCNKB Gene Bartter Syndrome Type 3 NGS Genetic DNA Test for INR 20000. This test can help diagnose the disease in individuals with symptoms or a family history of Bartter syndrome.

Symptoms of Bartter Syndrome Type 3

The symptoms of Bartter syndrome type 3 can vary in severity and may include:

• Polyuria (excessive urination)
• Polydipsia (excessive thirst)
• Dehydration
• Electrolyte imbalances
• Hypokalemia (low potassium levels)
• Hypocalcemia (low calcium levels)
• Hypomagnesemia (low magnesium levels)
• Growth and development delays

These symptoms can also lead to other health problems like muscle weakness, fatigue, seizures, and cognitive impairment.

Diagnosing Bartter Syndrome Type 3

Bartter syndrome type 3 is diagnosed through genetic testing. The CLCNKB Gene Bartter Syndrome Type 3 NGS Genetic DNA Test offered by DNA Labs India can identify mutations in the CLCNKB gene that cause the disease. This test is highly accurate and can detect mutations in the gene with a sensitivity of over 99%.

In addition to genetic testing, doctors may also perform other tests to evaluate electrolyte imbalances and kidney function. These tests can include blood tests, urine tests, and imaging studies.

Conclusion

Bartter syndrome type 3 is a rare genetic disorder that can cause a range of symptoms and health problems. NGS genetic DNA testing is a valuable tool that can help diagnose the disease and identify individuals who may be at risk. The CLCNKB Gene Bartter Syndrome Type 3 NGS Genetic DNA Test offered by DNA Labs India is a reliable and accurate test that can help individuals and families understand their risk of developing the disease and take appropriate steps to manage their health.

For more information about the CLCNKB Gene Bartter Syndrome Type 3 NGS Genetic DNA Test, contact DNA Labs India today.