Genetic Test Panels
Hereditary Cancer (CGX)
Cardiovascular Disease (CardioGX)
Cardiovascular Disease (CardioGX)
A (CGx) cancer genetic test identifies specific, inheritable gene mutations that may increase a patient's risk of developing or redeveloping cancer. Gain insight as this test will analyze genes and tumor markers, including BRCA1, BRCA2, ATM, COH1, MLH1, HSH2, MSH6, and PTEN. If a pathogenic variant is identified in your patient, close relatives (children, siblings, and parents) are up to 8 times more likely to also be at increased risk.
Cardiovascular Disease (CardioGX)
Cardiovascular Disease (CardioGX)
Cardiovascular Disease (CardioGX)
Inherited heart conditions are passed on through families and are caused by a change (or mutation) in one or more of a patient's genes. There are many types of inherited heart conditions, including:
- Cardiomyopathy
- Arrhythmia
- Arteriopathy
- Familial Hypercholesterolemia (FH)
Pharmacogenetics (PGX)
Cardiovascular Disease (CardioGX)
Parkinson's-Altzheimer's-Dementia (PAD)
Pharmacogenetics test (PGX) focuses on how your patient's body metabolizes drug enzymes and the results will provide you with useful insight as to which medications are more useful, less useful and those that are potentially harmful. Pharmacogenetics is the study of how people respond differently to drug therapy based upon their genetic makeup or genes.
Parkinson's-Altzheimer's-Dementia (PAD)
Parkinson's-Altzheimer's-Dementia (PAD)
Parkinson's-Altzheimer's-Dementia (PAD)
Parkinson’s disease, Alzheimer’s disease, and genetic disorders that cause dementia. Genes play a role in the development of many types of dementia. A patient with a parent or sibling with dementia such as Alzheimer’s disease has on average a higher risk of developing the same condition themselves. Genetic testing can show if a patient has a specific gene that puts them at risk for developing Alzheimer’s.
Diabetes-Obesity
Parkinson's-Altzheimer's-Dementia (PAD)
Genetic Counseling
Patients with a personal and/or family history suggestive of monogenic diabetes and obesity related disorders. These conditions may occur independently or as clinical features of a genetic syndrome. If a pathogenic variant is identified in your patient, close relatives (children, siblings, and parents) are up to 50% more likely to also be at increased risk.
Genetic Counseling
Parkinson's-Altzheimer's-Dementia (PAD)
Genetic Counseling
A genetic test that identifies a pathogenic variant is provided via a clinical laboratory report. Bio Genetics Laboratory provides genetic counseling services for both the doctor and the patient. Incorporating a pro-active risk screening and management protocol into the patient's ongoing plan of treatment can mitigate the health risks before they become life-threatening.