Price:
Rs. 19,950.00
Sample Type: EDTA BLOOD
Fasting Not Required
Notes: G0110
Frequently Asked Questions (FAQ's):
What is the Fabry Disease Gene Panel?
This test analyzes the GLA gene using next-generation sequencing at Metropolis Healthcare to detect mutations linked to Fabry disease.
Why is this test important?
It helps confirm the genetic cause of symptoms such as burning limb pain, kidney dysfunction, or heart involvement.
Which sample type is needed for the test?
EDTA blood is required for DNA extraction and sequencing.
How does Metropolis Healthcare perform this test?
Using high-quality NGS technology, Metropolis Healthcare accurately identifies pathogenic variants in the GLA gene.
Who should consider taking this test?
Individuals with suspected Fabry disease or a family history of the condition.
How long does it take to receive results?
The report is provided within the standard NGS processing timeline at Metropolis Healthcare.
Can this test guide treatment?
Yes, identifying the specific mutation helps clinicians plan enzyme replacement or targeted therapy.
Is genetic counselling recommended?
Genetic counselling is advised to understand inheritance patterns and implications for family members