Alkaptonuria Urine Qualitative Test
Introduction
The Alkaptonuria Urine Qualitative Test is a crucial diagnostic tool used to detect Alkaptonuria, a rare metabolic disorder characterized by the accumulation of homogentisic acid in the body. This condition is part of a group of disorders known as inborn errors of metabolism. Early detection through this test is vital for managing the disease effectively and preventing complications.
What the Test Measures
This test measures the presence of homogentisic acid in the urine. Elevated levels of this compound indicate a diagnosis of Alkaptonuria, which can lead to severe health issues if left untreated.
Who Should Consider This Test?
Individuals who exhibit symptoms such as darkening of urine, arthritis, or a family history of metabolic disorders should consider taking the Alkaptonuria Urine Qualitative Test. It is particularly recommended for:
- Children showing signs of metabolic disorders.
- Individuals with a family history of Alkaptonuria.
- Patients with unexplained joint pain or discoloration of urine.
Benefits of Taking the Test
Taking the Alkaptonuria Urine Qualitative Test offers several benefits:
- Early diagnosis of Alkaptonuria, allowing for timely intervention.
- Helps in monitoring the progression of the disease.
- Informs treatment options and lifestyle adjustments to manage symptoms effectively.
Understanding Your Results
Results from the Alkaptonuria Urine Qualitative Test will indicate whether homogentisic acid is present in your urine. A positive result suggests the need for further investigation and management of Alkaptonuria. It is essential to discuss your results with a healthcare professional for proper interpretation and guidance.
Test Details and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Alkaptonuria Urine Qualitative Test | 80,000 NGN | 140,000 NGN |
Booking the Test
To book the Alkaptonuria Urine Qualitative Test, please contact us at DNA Labs Nigeria. You can call or WhatsApp us at +2348077798758. Take the first step towards better health today!
Test Specifications
- Turnaround Time: Daily
- Sample Type: 10 mL (5 mL min.) aliquot of freshly voided urine in a sterile screw capped container. No preservative required. Wrap container in aluminium foil to protect from light. Ship refrigerated or frozen. Clinical and drug history must accompany sample.
- Pre-test Instructions: Wrap freshly voided urine in a container covered with aluminium foil to protect from light. Clinical and drug history must accompany sample.
- Specialty: Pediatrician, Physician
- Department: Genetic
- Method: Chemical
- Disease Type: Inborn errors of metabolism
