- Approved and certified by CLIA
- Committed staff ready to assist
- Utilizing state-of-the-art technology and methodologies
- Timely and accurate delivery of results
Our CGx carcinogenic test pinpoints certain hereditary gene mutations that could heighten a patient's likelihood of developing or recurring cancer. The test examines genes and tumor markers such as BRCA1, BRCA2, ATM, COH1, MLH1, HSH2, MSH6, and PTEN. If a harmful genetic variation is found in close relatives, like parents, children, or siblings, their risk could be up to 8 times higher.
Conditions affecting the heart can be passed down through generations, resulting from changes or mutations in a patient's genes. Various types of inherited heart conditions exist, such as Cardiomyopathy, Arrhythmia, Arteriopathy, and Familial Hypercholesterolemia (FH).
The PGX test examines how a patient's body processes drug enzymes. Its results offer valuable information about which medications may be more effective or have potential risks. Pharmacogenetics explores how individuals respond uniquely to drug therapy based on their genetic makeup or genes.
Primary immunodeficiencies are ongoing conditions where a part of the immune system doesn't work properly. These inherited disorders can impact individuals of any age or gender. Identifying the specific mutation in the responsible gene is crucial for effective treatment.
Neurocognitive testing enables you to measure your brain function against others of similar age and your own past performance. It helps assess how conditions like dementia, stroke, concussion, ADHD, and other potential brain issues impact your brain function. This information allows you and your healthcare provider or therapist to create a personalized treatment plan.
Our test investigates alterations in 112 genes associated with thyroid cancer, alongside clinical indications of congenital hypothyroidism or thyroid hormone resistance. Each alteration detected in a tumor is scored based on its connection to thyroid cancer, encompassing mutations, gene fusions, copy number changes, and gene expression variations.