Price:
Rs. 21,000.00
Sample Type: EDTA BLOOD
Fasting Not Required
Notes:G0333
Frequently Asked Questions (FAQ's):
What does the Klippel-Feil Syndrome Gene Panel test detect?
It detects mutations in genes responsible for vertebral fusion and related developmental abnormalities.
How does Metropolis Healthcare perform this test?
Metropolis Healthcare uses high-quality Next-Generation Sequencing (NGS) to analyze multiple genes from an EDTA blood sample.
Who should undergo this test?
Individuals with congenital cervical spine fusion, short neck, limited neck mobility, or associated anomalies may benefit from this test.
Why is genetic testing important for Klippel-Feil Syndrome?
It helps confirm the underlying cause, assess severity, and guide multidisciplinary management and monitoring.
Can this test help with family planning?
Yes, identifying the genetic mutation helps determine recurrence risks for future pregnancies.
How accurate are the results?
Metropolis Healthcare maintains strict quality standards and uses advanced sequencing platforms for reliable and clinically validated results.
Does this test identify associated conditions?
It may reveal gene defects linked to hearing loss, renal anomalies, and other congenital features.
How long does the testing process take?
Metropolis Healthcare typically provides results within a standard NGS reporting timeline, depending on the complexity of analysis