GM2 Gangliosidosis Quantitative Blood Tay Sachs Sandhoff Disease Test
The GM2 Gangliosidosis Quantitative Blood Tay Sachs Sandhoff Disease Test is a specialized diagnostic tool used to detect GM2 gangliosidosis, a group of inherited metabolic disorders that affect the nervous system. This test is essential for individuals who may be carriers of Tay-Sachs or Sandhoff disease, which can lead to severe neurological impairment if not identified early.
What the Test Measures/Detects
This test quantifies the levels of GM2 gangliosides in the blood, which are crucial for the proper functioning of nerve cells. Abnormal levels may indicate the presence of GM2 gangliosidosis, allowing for timely intervention and management.
Who Should Consider This Test
Individuals with a family history of Tay-Sachs or Sandhoff disease, or those displaying symptoms such as:
- Progressive weakness
- Loss of motor skills
- Seizures
- Vision and hearing loss
are advised to consider this test. Additionally, pediatricians may recommend testing for newborns in high-risk populations.
Benefits of Taking the Test
Taking the GM2 Gangliosidosis Test offers numerous benefits:
- Early diagnosis can lead to better management of symptoms.
- Informs family planning for at-risk couples.
- Provides clarity and peace of mind to families.
- Guides healthcare providers in tailoring treatment plans.
Understanding Your Results
Results from the GM2 Gangliosidosis Test will indicate the levels of GM2 gangliosides in the blood. Normal levels suggest no risk of GM2 gangliosidosis, while elevated levels may require further investigation or intervention. It’s important to discuss results with your healthcare provider for a comprehensive understanding.
Test Pricing
Discount Price | Regular Price |
---|---|
70,000 NGN | 100,000 NGN |
Booking the Test
To book the GM2 Gangliosidosis Quantitative Blood Tay Sachs Sandhoff Disease Test, please call or WhatsApp us at +2348077798758. We are here to assist you with scheduling and any questions you may have.
Additional Information
Turnaround Time: Sample collected daily by 4 PM; report available in 4 days.
Sample Type: 10 ml (7.5 mL min.) whole blood from 3 Lavender Top (EDTA) / Green Top (Sodium heparin) tubes. Ship refrigerated. DO NOT FREEZE. Clinical details must accompany the sample.
Pre-Test Instructions: Clinical details must accompany the sample.
Specialty: Pediatrician
Department: Genetic
Method: Enzyme Assay
Disease Type: Inborn Errors of Metabolism
Don’t wait for symptoms to arise. Ensure your family’s health and peace of mind by booking the GM2 Gangliosidosis Quantitative Blood Tay Sachs Sandhoff Disease Test today!