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India Gets Its First Non-Invasive FDA-Approved Test for Alzheimer’s Detection, Here's All You Need To Know

India Gets Its First Non-Invasive FDA-Approved Test for Alzheimer’s Detection, Here's All You Need To Know

Credits: Canva

Text
Ishita Roy

Updated Sep 23, 2025 | 05:00 PM IST
SummaryIndia has launched Dendrite Dx, its first FDA-approved non-invasive test for Alzheimer’s detection. Offered by Dr Dangs Labs, it combines a cognitive assessment, blood biomarkers, and an APS2 score to estimate amyloid plaque risk. Expected to cost around ₹10,000, the test enables early, reliable diagnosis, reducing dependence on invasive lumbar punctures or costly scans.

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