Studying Genetic Factors in Adults with Neurodegenerative Dementias or Family History at a Cognitive Clinic

What this Trial Is About

Researchers are investigating genetic factors that may contribute to neurodegenerative dementias such as Frontotemporal Dementia, Lewy Body Disease, and Alzheimers disease. The study aims to identify and understand genetic mutations or polymorphisms that could cause these conditions, especially in patients with suspected or confirmed neurodegenerative dementia or those with a family history of such disorders. Many genetic causes remain unknown, making this research important for uncovering potential genetic risks. Participants will undergo a one-time blood draw to collect biosamples for genetic testing. This involves a brief visit lasting approximately 20 minutes during which the genetic status or polymorphism results will be obtained. The study is observational and does not involve any treatment or intervention beyond the collection of blood samples. During the visit, demographic information, medical history, and clinical or pathological diagnoses will be recorded, typically within one month of the clinic visit. The study primarily measures genetic results from the blood sample, with additional data collected to support the research. Participants will have a single study visit, and no long-term follow-up is described. The total participation time is limited to about 20 minutes for the main procedures.

Investigating Genetic Status in Patients Presenting to Clinic