The Fanconi Anemia Gene Panel by NGS examines a wide range of genes involved in Fanconi anemia, a hereditary bone marrow failure and DNA-repair disorder. Using an EDTA blood sample, this test helps detect disease-causing variants that affect blood formation, chromosomal stability, and overall cellular health. Metropolis Healthcare employs advanced next-generation sequencing to ensure high accuracy and comprehensive gene coverage. The results support early diagnosis, clinical decision-making, family screening, and individualized patient management.
Price:
Rs. 21,000.00
Sample Type: EDTA BLOOD
Fasting Not Required
Notes:G0197
Frequently Asked Questions (FAQ's):
What does the Fanconi Anemia Gene Panel include at Metropolis Healthcare?
It analyzes multiple genes associated with Fanconi anemia and related DNA-repair disorders using high-quality NGS technology.
How does Metropolis Healthcare perform this test?
Metropolis Healthcare isolates DNA from EDTA blood and sequences the targeted genes using advanced next-generation sequencing platforms.
Who should consider taking this test at Metropolis Healthcare?
Individuals with bone marrow failure, congenital anomalies, unexplained pancytopenia, or a family history of Fanconi anemia may benefit from this panel.
What sample is required for this test at Metropolis Healthcare?
A standard EDTA blood sample is required for accurate and reliable DNA sequencing.
How long does Metropolis Healthcare take to deliver the results?
Turnaround time varies based on sequencing and analysis steps, with reports provided promptly once evaluation is completed.
Why choose Metropolis Healthcare for this genetic panel?
Metropolis Healthcare provides extensive gene coverage, stringent quality checks, and clinically meaningful interpretation of results.
Does Metropolis Healthcare offer post-test guidance?
Yes, results include expert genetic insights to help clinicians plan further evaluation and management.
Is this test suitable for children at Metropolis Healthcare?
Yes, the panel is appropriate for pediatric as well as adult patients when Fanconi anemia is suspected.