Niemann Pick Disease Quantitative Blood Test
Introduction
The Niemann Pick Disease Quantitative Blood Test is a crucial diagnostic tool for identifying Niemann Pick Disease, a rare genetic disorder that affects lipid metabolism. This test is particularly significant for pediatric patients as early detection can lead to timely intervention and management strategies.
What the Test Measures
This test quantitatively measures the levels of sphingomyelin in the blood, which is indicative of Niemann Pick Disease. Abnormal levels suggest a disruption in lipid metabolism, characteristic of this condition.
Who Should Consider This Test
Parents should consider this test for children exhibiting symptoms such as:
- Enlarged liver or spleen
- Neurological issues
- Developmental delays
- Recurrent infections
Additionally, children with a family history of Niemann Pick Disease or related metabolic disorders are at higher risk and should be screened.
Benefits of Taking the Test
- Early diagnosis can significantly improve management options.
- Helps in understanding the underlying cause of symptoms.
- Guides pediatricians in creating tailored treatment plans.
- Provides peace of mind for families regarding their child’s health.
Understanding Your Results
Upon receiving your test results, it is important to consult with a healthcare professional. They can explain the findings in the context of your child’s health and recommend further actions if necessary.
Test Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| Niemann Pick Disease Quantitative Blood Test | 51246 | 56940 |
Booking Information
To book the Niemann Pick Disease Quantitative Blood Test, please contact us at +2348077798758. Our team is ready to assist you with scheduling and any inquiries you may have.
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) / 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
