SCNN1G Gene Pseudohypoaldosteronism Type 1 Autosomal Recessive NGS Genetic DNA Test
Introduction
The SCNN1G Gene Pseudohypoaldosteronism Type 1 Autosomal Recessive NGS Genetic DNA Test is an advanced diagnostic tool used to identify genetic mutations associated with pseudohypoaldosteronism, a condition affecting sodium transport in the body. This test employs Next-Generation Sequencing (NGS) technology to provide accurate and comprehensive results, aiding in the diagnosis and management of related health issues.
What the Test Measures
This test detects mutations in the SCNN1G gene, which encodes a subunit of the epithelial sodium channel. Abnormalities in this gene can lead to sodium retention and other electrolyte imbalances, manifesting as various clinical symptoms.
Who Should Consider This Test?
Individuals experiencing symptoms such as:
- Severe dehydration
- Electrolyte imbalances
- Hypertension
- Family history of pseudohypoaldosteronism
should consider undergoing this genetic test. Additionally, those with a family history of related disorders may benefit from genetic counseling and testing.
Benefits of Taking the Test
- Early diagnosis of genetic conditions.
- Guidance for treatment options based on genetic findings.
- Informed family planning decisions through genetic counseling.
- Understanding personal health risks and management strategies.
Understanding Your Results
Results from the SCNN1G Gene Test will be interpreted by qualified healthcare professionals. A positive result may indicate a genetic predisposition to pseudohypoaldosteronism, while a negative result can provide reassurance. It is essential to discuss the implications of your results with a genetic counselor or your healthcare provider.
Test Details and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| SCNN1G Gene Pseudohypoaldosteronism Type 1 Autosomal Recessive NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book the Test
To book the SCNN1G Gene Pseudohypoaldosteronism Type 1 Autosomal Recessive NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you through the booking process and answer any questions you may have.
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: A clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected with this condition are recommended.
Our specialty in General Medicine, Genetics, and the use of NGS technology ensures you receive the highest quality of diagnostic services.
