Short Description

NGS genetic DNA test detecets for variant and mutation detection in CYP11B2 gene for Hypoaldosteronism, congenital, due to CMO II deficiency

PreTest Information

Clinical History of Patient who is going for CYP11B2 Gene Hypoaldosteronism, congenital, due to CMO II deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Hypoaldosteronism, congenital, due to CMO II deficiency

Detail Description

CYP11B2 Gene Hypoaldosteronism: Congenital Due to CMO II Deficiency NGS Genetic DNA Test

Are you experiencing symptoms of low blood pressure, muscle weakness, or dehydration? These could be signs of CYP11B2 Gene Hypoaldosteronism. This is a rare genetic disorder that affects the production of aldosterone, a hormone that regulates salt and water balance in the body.

CYP11B2 Gene Hypoaldosteronism is caused by a deficiency in the CMO II enzyme. This enzyme is responsible for the conversion of corticosterone to aldosterone in the adrenal glands. Without enough aldosterone, the body loses too much salt and water, leading to the symptoms mentioned above.

Symptoms

The symptoms of CYP11B2 Gene Hypoaldosteronism can vary from person to person, but some of the common symptoms include:

• Low blood pressure
• Muscle weakness
• Dehydration
• Abnormal heart rhythms
• Fatigue
• Headaches
• Nausea and vomiting

Diagnosis

Diagnosing CYP11B2 Gene Hypoaldosteronism can be challenging because it is a rare genetic disorder. However, doctors can perform various tests to determine if you have the condition. These tests may include:

• Blood tests to measure aldosterone and renin levels
• Urine tests to measure electrolyte levels
• Genetic testing to look for mutations in the CYP11B2 gene

NGS Genetic DNA Test

The NGS Genetic DNA Test is a comprehensive genetic testing solution that can detect mutations in the CYP11B2 gene. This test uses Next-Generation Sequencing (NGS) technology to analyze the entire gene, providing accurate and reliable results.

The cost of the NGS Genetic DNA Test for CYP11B2 Gene Hypoaldosteronism is INR 20,000. This test is covered by most insurance plans, and financing options are available for those who need it.

Conclusion

CYP11B2 Gene Hypoaldosteronism is a rare genetic disorder that can cause a range of symptoms, including low blood pressure, muscle weakness, and dehydration. If you are experiencing these symptoms, it is essential to speak with your doctor and consider genetic testing. The NGS Genetic DNA Test for CYP11B2 Gene Hypoaldosteronism is an accurate and reliable option that can provide you with the answers you need to manage your condition effectively.

Contact DNA Labs India today to learn more about our genetic testing solutions.