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Test · Diagnostics

NBS-49 Disorders

Free home sample collection, physician reviewed5 DaysReports inBloodSample

The NBS-49 test evaluates metabolite profiles in a dried blood spot using tandem mass spectrometry to detect 49 inherited metabolic and genetic disorders such as phenylketonuria, medium-chain acyl-CoA dehydrogenase deficiency, and classical galactosemia allowing early diagnosis and intervention to prevent severe complications.

₹2,400—Members pay ₹2160