This genetic test analyzes multiple genes associated with Marfan syndrome and related connective tissue disorders using Next Generation Sequencing (NGS).
It helps identify inherited mutations that may affect the heart, blood vessels, eyes, and skeletal system.
The test requires an EDTA blood sample for accurate DNA analysis.
Metropolis Healthcare offers this advanced genetic panel with high analytical precision and clinical reliability.
Price:
Rs. 22,050.00
Sample Type: EDTA BLOOD
Fasting Not Required
Notes: M0136
Frequently Asked Questions (FAQ's):
What does the MARFANS SYNDROME GENE PANEL BY NGS include?
This test includes comprehensive analysis of key genes linked to Marfan syndrome and similar hereditary connective tissue conditions, performed at Metropolis Healthcare laboratories.
How does Metropolis Healthcare perform this genetic test?
Metropolis Healthcare uses advanced NGS technology on an EDTA blood sample to detect clinically relevant genetic variations with high accuracy.
Who should take the MARFANS SYNDROME GENE PANEL BY NGS test?
This test is recommended for individuals with clinical features of Marfan syndrome, a family history of the condition, or unexplained cardiovascular or skeletal abnormalities.
Why is NGS used in this test at Metropolis Healthcare?
NGS allows Metropolis Healthcare to analyze multiple genes simultaneously, improving diagnostic yield and enabling early and precise genetic diagnosis.
Is genetic counseling advised with this test from Metropolis Healthcare?
Yes, Metropolis Healthcare strongly recommends genetic counseling before and after testing to help understand results and their clinical implications.
How is the EDTA blood sample collected for this test?
A trained Metropolis Healthcare professional collects a blood sample in an EDTA tube following standardized safety and quality protocols.
How can the results from Metropolis Healthcare help in patient management?
The results assist clinicians in confirming diagnosis, guiding treatment decisions, monitoring complications, and providing family screening recommendations