ABHD1 Gene Lung Alphabeta Hydrolase Deficiency Type 1 NGS Genetic DNA Test
Introduction
The ABHD1 Gene Lung Alphabeta Hydrolase Deficiency Type 1 NGS Genetic DNA Test is an advanced diagnostic test that utilizes Next Generation Sequencing (NGS) technology to detect mutations in the ABHD1 gene. This gene is crucial for the metabolism of certain lipids, and its deficiency can lead to significant metabolic disorders. Early detection through this test is vital for effective management and treatment, making it an essential tool for individuals at risk.
What the Test Measures
This genetic test specifically measures the presence of mutations in the ABHD1 gene, which can indicate a predisposition to lung alphabeta hydrolase deficiency type 1. By analyzing the DNA sequence, healthcare providers can determine whether an individual carries genetic variants that may affect their health.
Who Should Consider This Test?
This test is recommended for individuals who:
- Have a family history of metabolic disorders.
- Show symptoms related to lipid metabolism issues.
- Are seeking genetic counseling for personal or family planning purposes.
Benefits of Taking the Test
- Early identification of genetic predispositions allows for timely intervention.
- Informs healthcare providers about potential health risks.
- Guides treatment options and lifestyle changes to manage or mitigate risks.
- Provides valuable information for family planning and genetic counseling.
Understanding Your Results
Results from the ABHD1 Gene Lung Alphabeta Hydrolase Deficiency Type 1 NGS Genetic DNA Test will be provided along with a comprehensive report. It is important to discuss these results with a healthcare provider, who can explain the implications and recommend further actions based on the findings.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Book the Test
To book the ABHD1 Gene Lung Alphabeta Hydrolase Deficiency Type 1 NGS Genetic DNA Test, please call or WhatsApp us at +2348077798758. Our dedicated team is here to assist you with any inquiries and to guide you through the booking process.
Turnaround time for results is approximately 3 to 4 weeks, and the sample type required for this test is blood. Prior to the test, a genetic counseling session is recommended to gather a clinical history and create a pedigree chart of affected family members.
