Genetic testing for Wilson’s disease identifies inherited mutations that cause copper to accumulate in the liver, brain, and other organs….

Genetic testing for polycystic kidney disease (PKD) identifies inherited variants that influence kidney cyst formation, disease progression, and risk of…

Genetic testing for Parkinson’s disease helps identify inherited mutations that increase the risk of developing this progressive neurological condition. Understanding…

Genetic testing for pancreatic cancer supports identification of inherited risks, enables early surveillance, and guides decision‐making for patients and families…

Genetic testing for Lynch Syndrome helps families identify inherited risks for colorectal and other cancers, guiding early prevention, surveillance, and…

Genetic testing for IVF, known as preimplantation genetic testing (PGT), helps identify healthy embryos before transfer to the uterus. By…

Hemochromatosis genetic testing identifies inherited mutations that cause excessive iron accumulation in the body, particularly in the liver, heart, and…

Familial hypercholesterolemia (FH) genetic testing identifies inherited changes that cause extremely high cholesterol levels, often from birth. Understanding these genetic…

Genetic testing for epilepsy reveals inherited variations that influence how and why seizures develop, progress, and respond to treatment. By…

Genetic testing for dementia helps reveal inherited mutations that influence how, when, and why different forms of dementia develop. By…