The Rasopathy Gene Panel analyzes multiple genes associated with Ras-MAPK pathway disorders using advanced Next-Generation Sequencing (NGS) on an EDTA blood sample. Metropolis Healthcare performs this high-precision test to help diagnose conditions such as Noonan syndrome, Costello syndrome, and related developmental disorders. The panel aids in identifying the genetic cause of congenital anomalies, cardiac defects, and growth abnormalities. It supports early diagnosis, clinical management, and informed family counseling.
Price:
Rs. 21,000.00
Sample Type: EDTA BLOOD
Fasting Not Required
Notes:G0246
Frequently Asked Questions (FAQ's):
What does the Rasopathy Gene Panel include?
The Rasopathy panel at Metropolis Healthcare includes comprehensive sequencing of genes involved in the Ras-MAPK pathway linked to syndromes like Noonan and Costello.
How does Metropolis Healthcare perform this test?
Metropolis Healthcare uses high-depth NGS technology to detect disease-causing variants with high accuracy and reliability.
Who should take this test?
Individuals with unexplained developmental delays, congenital heart defects, craniofacial differences, or suspected Rasopathy syndromes may benefit from this test at Metropolis Healthcare.
Why is this genetic test important?
This test helps confirm a clinical diagnosis, guides treatment decisions, and supports long-term management through accurate genetic insights from Metropolis Healthcare.
What type of sample is required?
An EDTA blood sample is collected, and Metropolis Healthcare isolates DNA for sequencing and variant analysis.
Can this test be used for pediatric cases?
Yes, the test is frequently recommended at Metropolis Healthcare for infants and children showing features associated with Rasopathies.
How long does it take to receive results?
Metropolis Healthcare strives to deliver detailed and accurate reports within a standard genetic testing turnaround time.
Does this test help with genetic counseling?
Yes, Metropolis Healthcare provides results that assist families in understanding inheritance patterns and future reproductive risks.