A comprehensive DNA test that screens 35 genes linked to Alzheimer's, Parkinson's, frontotemporal dementia, and inherited movement disorders.


Alzheimer's disease
Genes linked to inherited Alzheimer's disease. PSEN1 and PSEN2 cause rare early-onset forms, while APOE affects risk for the more common late-onset form.
Parkinson's disease
Genes tied to typical-onset Parkinson's disease. LRRK2 and GBA are the most common genetic risk factors and are actively being targeted by new therapies.
Young-onset Parkinson's & parkinsonism
Genes behind Parkinson's that starts before age 50. These tend to be recessive (inherited from both parents) and often progress more slowly.
Frontotemporal dementia & ALS overlap
Genes behind frontotemporal dementia (FTD), which affects personality and language. C9orf72 can cause both FTD and ALS in the same family.
Rare movement & dystonia disorders
Genes causing inherited dystonia and movement disorders. Some, like GCH1, respond very well to medication when diagnosed.
Rare inherited dementias
Genes behind rare forms of inherited dementia, including prion disease, CADASIL (small vessel strokes), and white matter disorders.
Know your genetic risks. Share with your doctor. Plan ahead with confidence.