Orotic Acid Test
Introduction to the Orotic Acid Test
The Orotic Acid Test is a vital diagnostic tool used in the field of genetics and metabolic disorders. It is particularly significant in identifying inborn errors of metabolism, which can lead to serious health complications if undiagnosed. By measuring the levels of orotic acid in urine, healthcare providers can gain crucial insights into a patient’s metabolic function, especially in pediatric populations.
What the Test Measures
This test specifically measures the concentration of orotic acid in a random urine sample. Elevated levels of orotic acid can indicate metabolic disorders such as Ornithine Transcarbamylase Deficiency and other urea cycle disorders.
Who Should Consider This Test?
Parents or guardians should consider the Orotic Acid Test for children displaying symptoms such as:
- Developmental delays
- Unusual lethargy or fatigue
- Vomiting or feeding difficulties
- Failure to thrive
Additionally, individuals with a family history of metabolic disorders may also benefit from this test.
Benefits of Taking the Test
- Early detection of metabolic disorders can lead to timely intervention.
- Helps in managing symptoms and preventing complications.
- Provides peace of mind for families with a history of metabolic issues.
Understanding Your Results
Upon receiving your test results, it is essential to consult with a healthcare professional who can interpret the findings accurately. Elevated orotic acid levels may require further testing or evaluation to confirm a diagnosis and determine the best course of action.
Pricing Information
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| Orotic Acid Test | 100,000 NGN | 160,000 NGN |
Booking Your Test
To book the Orotic Acid Test, please contact us at DNA Labs Nigeria. We are committed to providing high-quality diagnostic services to our patients. Call or WhatsApp us at +2348077798758 to schedule your appointment.
Test Details
Turnaround Time: Sample Mon / Thu by 9 am; Report Thu / Mon
Sample Type: 15 mL (10 mL min.) aliquot of random urine. Ship refrigerated or frozen. Collect specimen fasting or 2-3 hours post-feed. Provide a brief clinical history.
Method: GC-MS
Department: Genetic
Specialty: Pediatrician
Disease Type: Inborn Errors of Metabolism
