Parkinson's Disease Research Registry; establish within State Department of Health.

Summary

The bill would set up a Mississippi Parkinson's Disease Research Registry within the State Department of Health and require movement‑disorder centers and providers to report each Parkinson's case starting in 2027. An advisory committee of clinicians, researchers, a patient and public‑health experts would guide the registry, which would collect confidential epidemiological data. Researchers could request de‑identified data with IRB approval, while patients could opt out of the registry.

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