CYP11B2 Gene Hypoaldosteronism Congenital Due to CMO I Deficiency NGS Genetic DNA Test
Introduction
The CYP11B2 Gene Hypoaldosteronism Congenital Due to CMO I Deficiency NGS Genetic DNA Test is a vital diagnostic tool for identifying genetic conditions that affect aldosterone production in the body. By utilizing Next Generation Sequencing (NGS) technology, this test provides comprehensive insights into genetic predispositions related to metabolic disorders.
What the Test Measures
This genetic test specifically measures mutations in the CYP11B2 gene, which is responsible for producing the enzyme that converts cholesterol into aldosterone. Abnormalities in this gene can lead to congenital hypoaldosteronism, impacting blood pressure regulation and electrolyte balance.
Who Should Consider This Test
Individuals who may benefit from the CYP11B2 Gene Hypoaldosteronism test include:
- Patients with symptoms of low aldosterone levels such as fatigue, dizziness, or dehydration.
- Individuals with a family history of metabolic disorders.
- Patients experiencing unexplained electrolyte imbalances.
Benefits of Taking the Test
The benefits of undergoing the CYP11B2 Gene Hypoaldosteronism NGS Genetic DNA Test include:
- Accurate identification of genetic mutations that may affect health.
- Guidance for personalized treatment plans based on genetic findings.
- Enhanced understanding of potential health risks for affected individuals and their families.
Understanding Your Results
Results from the CYP11B2 Gene test will provide insights into whether specific mutations are present. It is essential to consult with a healthcare professional to interpret the results accurately and discuss potential next steps.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| CYP11B2 Gene Hypoaldosteronism NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Sample Type and Instructions
The test requires a sample of blood or extracted DNA, or even one drop of blood on an FTA card. Prior to testing, a clinical history and genetic counselling session are recommended to create a pedigree chart of family members affected by hypoaldosteronism.
Branches and Booking
DNA Labs has branches across all major cities in Kenya, making it convenient for you to access our services. To book the CYP11B2 Gene Hypoaldosteronism Congenital Due to CMO I Deficiency NGS Genetic DNA Test, please call or WhatsApp us at +254711564616. Don’t delay in taking control of your health!
