Pharmacogenomics (PGX)

Everyone has a unique genetic makeup. This can affect how you will respond or react to certain medications.Using the results from PGx testing, health care providers can individualize drug therapy selection and dosages for patients based on their genetic makeup. Testing patients prior to beginning treatment may help determine their response to certain drug classes and help avoid drugs that may be ineffective or cause harmful side effects. For patients currently on treatment, it may identify new treatment options or identify why current treatments aren’t working.

Hereditary Cancer

Our comprehensive hereditary cancer tests up to 127 genes associated with potential risk for hereditary cancer syndromes, helping identify individuals at risk for developing certain cancers or other health conditions. Results from this test can help define the best treatment and management plan based on the individual’s risk. Early detection is the key to being proactive about your health!

Cardiovascular

Our comprehensive cardiovascular panel covers a broad spectrum of inherited heart conditions and diseases, examining 252 different genes related to cardiovascular health, indicating diseases such as cardiomyopathy, arrhythmia, vascular & connective tissue diseases, congenital & pediatrics cardiovascular-related diseases, & more.

Neurological

Genetic testing for neurological disorders involves analyzing an individual’s DNA to identify genetic variations that may contribute to or cause a neurological condition. The types of genetic testing available include diagnostic testing, which looks for specific mutations in 164 genes known to cause disorders such as Parkinson’s Disease, Huntington’s Disease, Epilepsy, Alzheimer’s Disease and many others.

 

Primary Immunodeficiency

This panel tests for mutations in 47 genes and may be appropriate for anyone who has a personal history of frequent infections, fevers, or rash, particularly if infections do not completely clear up or keep coming back, require hospitalization or IV antibiotics, or are caused by an uncommon organism. Associated conditions include but are not limited to:

  • Adenosine deaminase Deficiency
  • Agammaglobulinemia (x-linked and autosomal recessive)
  • Ataxia telangiectasia
  • Chronic granulomatous disease
  • Immunoglobulin A Deficiency
  • Wiskott-Aldrich syndrome
  • IgE syndrome
  • X-linked SCID (severe combined immunodeficiency)

Hereditary Thyroid Disease

Genetic testing for thyroid disease is a type of 46-panel testing that looks for changes or mutations in a person’s DNA that may indicate an increased risk of developing thyroid disorders such as thyroid cancer, thyroid nodules, hyperthyroidism, or hypothyroidism. It can also help guide treatment decisions and identify family members who may be at risk for developing these conditions.

 

ADDITIONAL TESTS

  • CFR CPR
  • Wound PCR
  • Nail PCR
  • GI PCR
  • Toxicology Drug Testing Confirmation
  • Toxicology Screen (UDS)
  • STI PCR (Sexually-Transmitted   Infections)
  • UTI PCR
  • UTI+STI PCR
  • UA (Urinalysis)
  • UA with Confirmation/Reflex
  • Bloodwork