Price:
Rs. 21,000.00
Sample Type: EDTA BLOOD
Fasting Not Required
Booking Procedure:
- Technician from Metropolis will be assigned for a home sample collection after booking confirmation.
- Sample will be collected by our technician at your address at given slot.
- You can make the payment to the technician at the time of collection
- Your sample will then be transported to the nearest collection center and will be centrifuged before sending to the lab for processing.
- Soft copy reports will be sent to your email address within 24 to 48 hours or as per defined TAT for Tests.
Frequently Asked Questions (FAQ's):
What does the NCL Gene Panel by NGS include?
This panel covers key genes linked to different types of neuronal ceroid lipofuscinosis, analyzed with high-depth sequencing at Metropolis Healthcare.
How does Metropolis Healthcare perform this test?
Metropolis Healthcare uses next-generation sequencing to accurately detect pathogenic variants and ensure high-quality genomic interpretation.
Who should consider taking this test?
Individuals with symptoms like seizures, cognitive decline, motor difficulties, or early vision problems may benefit from this evaluation at Metropolis Healthcare.
Why is genetic testing important for suspected NCL cases?
Genetic confirmation helps classify the specific NCL type, enabling Metropolis Healthcare to support proper treatment planning and counseling.
What sample is required for this test at Metropolis Healthcare?
A simple EDTA blood sample is sufficient for performing the NGS-based analysis.
How long does it take to receive the results?
Metropolis Healthcare generally provides results within a few weeks, depending on sequencing and analysis requirements.
Can this panel detect both childhood and adult-onset NCL forms?
Yes, the test covers genes associated with various NCL subtypes, enabling Metropolis Healthcare to identify early- and late-onset forms.
Does Metropolis Healthcare offer support after receiving the results?
Yes, counseling and expert interpretation are available to help families understand the diagnosis and explore next steps