Mucopolysaccharidosis MPS Type VI Maroteaux Lamy Quantitative Blood Test
Introduction
The Mucopolysaccharidosis MPS Type VI Maroteaux Lamy Quantitative Blood Test is a specialized diagnostic tool used to identify deficiencies in the enzyme that breaks down mucopolysaccharides. This test is crucial for diagnosing Mucopolysaccharidosis (MPS) Type VI, a rare genetic disorder that affects the body’s ability to metabolize certain carbohydrates. Early detection through this test can lead to better management and treatment options for affected individuals.
What the Test Measures
This test specifically measures the levels of the enzyme arylsulfatase B in the blood. A deficiency in this enzyme can lead to the accumulation of harmful substances in the body, resulting in various health complications.
Who Should Consider This Test
Individuals showing symptoms such as skeletal abnormalities, joint stiffness, or developmental delays should consider this test. Additionally, those with a family history of MPS or related genetic disorders may be advised to undergo testing as a precautionary measure.
Benefits of Taking the Test
- Early diagnosis of MPS Type VI can lead to timely intervention and management.
- Helps in understanding the metabolic profile of the patient.
- Provides essential information for genetic counseling and family planning.
- Can guide treatment decisions to improve quality of life.
Understanding Your Results
Results from the Mucopolysaccharidosis MPS Type VI Maroteaux Lamy Quantitative Blood Test are typically available within four days. A healthcare provider will help interpret these results, explaining any deficiencies and the implications for treatment and management.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 38,376 NGN |
| Regular Price | 42,640 NGN |
Booking the Test
To book the Mucopolysaccharidosis MPS Type VI Maroteaux Lamy Quantitative Blood Test, please contact us at +2348077798758. Our team is ready to assist you with any inquiries and to schedule your appointment.
Test Details
Turnaround Time: Sample Daily by 4 PM; Report in 4 days
Sample Type: 10 mL (7.5 mL min.) whole blood from 3 Lavender Top (EDTA) OR Green Top (Sodium Heparin) tubes. Ship refrigerated. DO NOT FREEZE. Provide brief clinical history.
Pre-test Instructions: Provide brief clinical history.
Specialty: Pediatrician | Department: Genetic | Method: Enzyme assay | Disease Type: Inborn errors of metabolism
