Prader-Willi Syndrome-MS PCR
Overview of Prader-Willi Syndrome-MS PCR in Chandigarh
What is the Prader-Willi Syndrome MS-PCR test?
This molecular test detects genetic abnormalities associated with Prader-Willi syndrome, a rare disorder affecting growth, metabolism, and behavior.
Why is this test performed?
It is used to confirm a diagnosis in individuals with symptoms like poor muscle tone, excessive appetite, and developmental delays.
How is the test conducted?
A blood sample is analyzed using methylation-sensitive PCR (MS-PCR) to detect deletions or imprinting errors in the 15q11-q13 region.
What do abnormal results indicate?
A positive test confirms Prader-Willi syndrome, providing crucial information for genetic counseling and management.
What are the next steps if the test is positive?
A multidisciplinary approach involving hormone therapy, dietary management, and behavioral therapy is recommended.
Test included
- Specimen Source
- Preliminary Report
- Prader-willi Syndrome-ms Pcr
Doctor information
Test code
RD1418
CPT and Loinc codes
Department
- Advanced Molecular Diagnostics R&d
Turn around time
8 Working Days
Test run frequency
Every Day TIME - 09:30
Performing locations
2 labs across India
Specimen vol. and vacutainer information
| Specimen | Vacutainer | Volume |
|---|---|---|
| Edta Whole Blood | Lavender Vacutainer | 3 ml |
Specimen stability information
Edta Whole Blood
Collection instructions
Clinical History
Package price
₹7200
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₹7200