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Laboratory

Exult Diagnostics, Dr. Lal PathLabs

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FISH: PRADER WILLI SYNDROME / SNRPN

 6400

EX0700      FISH: PRADER WILLI SYNDROME / SNRPN
Specimen: 5 mL (3 mL min.) Whole blood from 1 Green Top (Sodium Heparin) tube. Ship at 18-22°C. DO NOT FREEZE.
Stability:
Room Refrigerated Frozen
48 hrs NA NA
Method: FISH
Comment: Samples received on holidays will be reported in the next schedule / next working day.
Report: Contact us to know the TAT.
Usage: Prader-Willi Syndrome (PWS) is a genetic disorder caused by the loss of function of specific genes on the proximal arm of chromosome 15. Most cases (99%) are caused by the absence of a paternal contribution to the imprinted region on chromosome 15q11-q13; approximately 70% of these are due to a large 5-7 Mb deletion. These patients are constantly hungry (hyperphagia) & become obese. They have behavioral, cognitive & sleep impairment and underdeveloped sex organs.
Doctor Specialty: Pediatrician
Disease: Genetic Disorders
Components:
Courier Charges: 0.00
Home Collection: Available (*T&C Apply)
Department: CYTOGENETICS
Pre Test Information: A duly filled Chromosome & FISH analysis Requisition Form is mandatory.