Price:
Rs. 7,420.00
Sample Type: EDTA Blood
Fasting Not Required
Notes: P1008
Frequently Asked Questions (FAQ's):
What does the Prader–Willi / Angelman Syndrome test detect?
It identifies chromosomal abnormalities or imprinting defects on chromosome 15 linked to these syndromes.
How does Metropolis Healthcare perform this test?
Metropolis Healthcare uses advanced molecular and genetic assays to accurately detect deletions or methylation abnormalities.
Who should take this test?
Infants or children with developmental delay, low muscle tone, feeding difficulties, or features suggestive of these syndromes may need this test.
What sample is required?
A blood sample collected in an EDTA tube is used for the analysis.
Is fasting needed before giving the sample?
No, fasting or special preparation is not required.
Can this test differentiate between Prader–Willi and Angelman syndrome?
Yes, the specialized techniques at Metropolis Healthcare help distinguish between the two conditions.
Are results useful for family planning?
Yes, results provide important information for genetic counseling and future risk assessment.
How long does it take to get the report?
Genetic tests may take longer; Metropolis Healthcare provides the report within the standard molecular testing timeframe.