Short Description

NGS genetic DNA test detecets for variant and mutation detection in GATA3 gene for Hypoparathyroidism, sensorineural deafness, and renal dysplasia

PreTest Information

Clinical History of Patient who is going for GATA3 Gene Hypoparathyroidism, sensorineural deafness, and renal dysplasia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GATA3 Gene Hypoparathyroidism, sensorineural deafness, and renal dysplasia NGS Genetic DNA Test gene GATA3

Detail Description

GATA3 Gene Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia NGS Genetic DNA Test

Genetic testing is becoming increasingly popular as a means of diagnosing inherited diseases. One such genetic disorder is GATA3 gene hypoparathyroidism, sensorineural deafness, and renal dysplasia. This disorder is caused by a mutation in the GATA3 gene, which is responsible for regulating the development of certain organs in the body.

Symptoms

The symptoms of GATA3 gene hypoparathyroidism, sensorineural deafness, and renal dysplasia can vary widely from person to person. Some individuals may experience only mild symptoms, while others may have more severe symptoms. The most common symptoms of this disorder include:

• Hypoparathyroidism – a condition in which the parathyroid gland does not produce enough parathyroid hormone, resulting in low levels of calcium in the blood
• Sensorineural deafness – a type of hearing loss caused by damage to the inner ear or the nerve that transmits sound from the ear to the brain
• Renal dysplasia – a condition in which the kidneys do not develop properly, leading to kidney failure

Diagnosis

Diagnosing GATA3 gene hypoparathyroidism, sensorineural deafness, and renal dysplasia can be challenging, as the symptoms can be similar to those of other conditions. A genetic test is the most reliable way to diagnose this disorder. This test involves analyzing a sample of the patient's DNA to look for mutations in the GATA3 gene. If a mutation is found, the patient is diagnosed with GATA3 gene hypoparathyroidism, sensorineural deafness, and renal dysplasia.

NGS Genetic DNA Test

Next-generation sequencing (NGS) is a powerful genetic testing technology that allows for the rapid and accurate analysis of large amounts of DNA. This technology can be used to analyze the GATA3 gene for mutations associated with hypoparathyroidism, sensorineural deafness, and renal dysplasia. The cost of this test is approximately INR 20,000.

Conclusion

GATA3 gene hypoparathyroidism, sensorineural deafness, and renal dysplasia is a rare genetic disorder that can cause a variety of symptoms. If you or a loved one is experiencing symptoms of this disorder, it is important to seek medical attention and consider genetic testing. The NGS genetic DNA test is a reliable and effective way to diagnose this disorder and can help patients receive the appropriate treatment and care.

At DNA Labs India, we offer a wide range of genetic testing services, including the NGS genetic DNA test for GATA3 gene hypoparathyroidism, sensorineural deafness, and renal dysplasia. Our team of experienced genetic counselors and scientists can help you understand the testing process and results, and provide you with the support you need throughout the process. Contact us today to learn more.