Our comprehensive testing panels may include genetic causes associated with: ●Alzheimer's Disease and other forms of dementia ●Frontotemporal Dementia (FTD) ●Parkinson's Disease ●Huntington's Disease ●Amyotrophic Lateral Sclerosis (ALS) ●Hereditary Ataxias ●Epilepsy and seizure disorders ●Autism Spectrum Disorder (ASD) ●Intellectual and developmental disabilities ●Other inherited neurological conditions

●Individuals with symptoms suggestive of a neurological disorder ●Those with a family history of dementia, Parkinson's disease, or other neurological conditions ●Families seeking to understand inherited risks ●Individuals considering predictive or presymptomatic testing ●Parents investigating potential genetic causes of neurodevelopmental conditions

●Supports accurate diagnosis and clinical management ●Identifies inherited risk factors ●Assists with family planning decisions ●Helps inform treatment and surveillance strategies ●Provides clarity for patients and their families

Using a blood or saliva sample, advanced genetic sequencing technology analyses genes associated with neurological and neurodevelopmental conditions. Results are interpreted by experienced specialists and may be accompanied by genetic counselling to help you understand the findings and available options. Understanding your genetics can provide valuable answers, guide healthcare decisions, and help families plan for the future with greater confidence.