Medical Genetics and Genomics Test for Neurological Disorders

Test is recommended for patients with high risk for neurological  disorders

Using NGS technology to analyze whole exome (the protein-encoding regions of 24,000 genes) with high coverage depth of  200X.

Medically certified genomics tests performed by US-certified medical geneticists (Fellows of American College of Medical Genetics and Genomics)

Detects germline variants that increase risk for neurological conditions, for instance, neurodevelopment disorders, movement disorders, neuromuscular disorders, neurodegenerative disorders, intellectual disability, epilepsy/seizure disorders, inherited eye disorders, cardiomyopathy and neuropathy, Alzheimer, Parkinson, dementia,... and other hereditary neurological conditions.

Confirmation analysis with gold standard tests using Microarray (Illumina iScan) and Sanger Sequencing

Test reports provide valuable information for screening and treatment of genetic neural disorders