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 Peroxisomal Disorder Gene Panel include?
It includes extensive gene sequencing performed by Metropolis Healthcare to detect mutations affecting peroxisome formation and metabolic activity.
How does Metropolis Healthcare perform this test?
Metropolis Healthcare uses high-accuracy NGS platforms to sequence multiple metabolism-related genes from an EDTA blood sample.
Who should take this test?
Infants, children, or adults with developmental delays, seizures, liver dysfunction, or suspected metabolic disorders may benefit.
Can this test confirm a peroxisomal disorder?
Yes, it helps identify specific genetic defects that confirm various peroxisomal biogenesis and enzyme-related disorders.
What sample is required for this test?
An EDTA blood sample is required to extract DNA for detailed genetic sequencing.
Is this test useful for family counseling?
Yes, identifying the genetic mutation helps determine inheritance patterns and assess recurrence risks in families.
How long does Metropolis Healthcare take to provide results?
Results typically take a few weeks due to complex sequencing and expert interpretation.
Does this test help guide clinical management?
Yes, genetic confirmation supports early intervention, monitoring, and personalized care planning for affected individuals