PRADER / WILLI SYNDROME-FISH
PRADER / WILLI SYNDROME-FISH

A “FISH” (fluorescent in-situ hybridization) test will identify those patients with PWS due to a deletion, but it will not identify those who have Prader-Willi syndrome by “UPD” (uniparental disomy) or an imprinting error. Almost all cases of PWS can be confirmed by one of the above tests.

Sample Type - Blood

Reporting Time - 6 Days

Prerequisites - No special preparation required

Price - ₹9080/-

Add to cart Go Home