Arginase Test
Introduction to the Arginase Test
The Arginase Test is a crucial diagnostic procedure aimed at identifying arginase deficiency, a rare genetic disorder that affects the body’s ability to metabolize certain proteins. This test plays a significant role in the early detection of inborn errors of metabolism, which can lead to severe health complications if left untreated. Early diagnosis through the Arginase Test can facilitate timely intervention, thus improving patient outcomes.
What the Test Measures
The Arginase Test measures the activity level of the enzyme arginase in the blood. Arginase is essential for the urea cycle, a process that helps eliminate ammonia from the body. Low levels of this enzyme can indicate a deficiency that may lead to a build-up of toxic substances, causing various metabolic disorders.
Who Should Consider This Test?
This test is recommended for individuals who exhibit symptoms such as:
- Neurological issues
- Developmental delays
- Unexplained hyperammonemia
- Familial history of metabolic disorders
Risk factors include a family history of inborn errors of metabolism or presenting symptoms that suggest metabolic dysfunction.
Benefits of Taking the Test
Taking the Arginase Test offers several benefits:
- Early diagnosis of metabolic disorders
- Guidance for treatment options
- Informed decision-making for family planning
- Peace of mind for patients and families
Understanding Your Results
Results from the Arginase Test will indicate the level of arginase enzyme activity in your blood. Normal results suggest proper metabolic function, while low activity levels may necessitate further investigation or intervention. It is essential to discuss your results with your healthcare provider for a comprehensive understanding and next steps.
Test Pricing
| Test Name | Price (NGN) |
|---|---|
| Arginase Test | Discount Price: 60,000 NGN |
| Regular Price: 120,000 NGN |
Book Your Test Today!
Ready to take the next step? Book the Arginase Test now to ensure your health and well-being. For inquiries or to schedule your test, please call or WhatsApp us at +2348077798758. Our team is here to assist you!
Turnaround Time: Sample must be submitted by 4 PM on Monday; report available by Thursday.
Sample Type: 4 mL (3 mL min.) whole blood from 1 Lavender Top (EDTA) tube. Ship refrigerated. DO NOT FREEZE.
Pre-Test Instructions: No special preparation required.
Specialty: Pediatrician
Department: Genetic
Method: Spectrophotometry
Disease Type: Inborn errors of metabolism
