FISH - Prader Willi Syndrome SNRPN
Prader-Willi Syndrome (PWS) is a genetic disorder caused by loss of function of specific genes on proximal arm of chromosome 15. Most cases (99%) are caused by 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 behavioural, cognitive & sleep impairment and underdeveloped sex organs.
Parameter(s) covered : 2
Report Frequency: Sample Daily by 4 pm; Report 7 Working days
Special Instruction: Duly filled Chromosome & FISH analysis Requisition Form (Form 17) is mandatory.
Price : ₹ 6900.00
Parameters
- Prader willi syndrome SNRPN
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