Price:
Rs. 21,000.00
Sample Type: EDTA BLOOD
Fasting Not Required
Notes:G0238
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