| Laboratory | Exult Diagnostics, Dr. Lal PathLabs, Metropolis Labs, Oncquest Labs, Pathkind Labs |
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Price range: ₹ 6400 through ₹ 16000
| EX1739 PRADER-WILLI SYNDROME MUTATION DETECTION METHYLATION SPECIFIC PCR | |||||||
| Specimen: | 4 mL (2 mL min.) whole blood in 1 Lavender top (EDTA) tube. Ship refrigerated. DO NOT FREEZE. | ||||||
| Stability: |
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| Method: | Methylation-specific PCR | ||||||
| Comment: | |||||||
| Report: | Contact us to know the TAT. | ||||||
| Usage: | Prader-Willi syndrome (PWS) and Angelman syndrome (AS) are clinically distinct neurodevelopmental genetic disorders that map to 15q11-q13. The primary phenotypes are attributable to the loss of expression of imprinted genes within this region which can arise by means of a number of mechanisms. The most sensitive single approach to diagnosing both PWS and AS is to study methylation patterns within 15q11-q13. | ||||||
| Doctor Specialty: | Pediatrician | ||||||
| Disease: | Genetic disorders | ||||||
| Components: | |||||||
| Courier Charges: | 0.00 | ||||||
| Home Collection: | Available (*T&C Apply) | ||||||
| Department: | MOLECULAR DIAGNOSTICS | ||||||
| Pre Test Information: | A duly filled Genomics Clinical Information Requisition Form is mandatory. | ||||||
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