Short Description

NGS genetic DNA test detecets for variant and mutation detection in SCNN1G gene for Pseudohypoaldosteronism, type 1, autosomal recessive

PreTest Information

Clinical History of Patient who is going for SCNN1G Gene Pseudohypoaldosteronism, type 1, autosomal recessive NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SCNN1G Gene Pseudohypoaldosteronism, type 1, autosomal recessive NGS Genetic DNA Test gene SCNN1G

Detail Description

SCNN1G Gene Pseudohypoaldosteronism - Symptoms, Diagnosis, and NGS Genetic DNA Test Cost

SCNN1G gene pseudohypoaldosteronism, type 1, autosomal recessive is a rare genetic disorder that affects the regulation of salt and water balance in the body. This disorder is caused by mutations in the SCNN1G gene, which provides instructions for making a protein that helps regulate salt and water balance in the kidneys.

Symptoms

The symptoms of SCNN1G gene pseudohypoaldosteronism, type 1, autosomal recessive can vary widely depending on the severity of the disorder. Some common symptoms include:

• Dehydration
• Low blood pressure
• Frequent urination
• Failure to thrive in infants
• Delayed growth and development
• Electrolyte imbalances

Diagnosis

SCNN1G gene pseudohypoaldosteronism, type 1, autosomal recessive is diagnosed through genetic testing. This may involve a variety of tests, including:

• NGS genetic testing
• Sanger sequencing
• PCR testing
• Whole exome sequencing

These tests can help identify mutations in the SCNN1G gene and confirm a diagnosis of the disorder. It is important to consult a genetic counselor or healthcare provider for guidance on testing options and interpretation of test results.

NGS Genetic DNA Test Cost

The cost of NGS genetic DNA testing for SCNN1G gene pseudohypoaldosteronism, type 1, autosomal recessive can vary depending on the provider and location. In India, the cost for this test is typically around INR 20,000. It is important to check with the provider for any additional fees or insurance coverage options.

Conclusion

SCNN1G gene pseudohypoaldosteronism, type 1, autosomal recessive is a rare genetic disorder that affects salt and water balance in the body. Symptoms can vary widely and diagnosis is confirmed through genetic testing. NGS genetic DNA testing for this disorder typically costs around INR 20,000 in India. It is important to consult a healthcare provider or genetic counselor for guidance on testing options and interpretation of test results.

If you suspect you or a loved one may have SCNN1G gene pseudohypoaldosteronism, type 1, autosomal recessive, it is important to seek medical attention and consider genetic testing for a proper diagnosis and treatment plan.

At DNA Labs India, we offer a wide range of genetic testing options including NGS genetic DNA testing for SCNN1G gene pseudohypoaldosteronism, type 1, autosomal recessive. Our team of experienced professionals is dedicated to providing accurate and timely results to help guide healthcare decisions. Contact us today to learn more about our testing options and how we can help.

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 SCNN1G Gene Pseudohypoaldosteronism, type 1, autosomal recessive NGS Genetic DNA Test