What If a Disease
Could Be Stopped
Before It Starts?
The Hidden Risks You Cannot See
Many chronic and hereditary diseases remain silent for years. Without preventive testing, early warning signs go undetected until serious health challenges arise. Understanding these risks early is key to proactive health management and informed decision-making.
Next Generation Sequencing (NGS) genetic testing evaluates hundreds of genes at once to identify inherited risks for conditions such as cardiomyopathy, metabolic disorders, cancer predisposition, and neurodegenerative diseases. Early detection through NGS allows individuals to take preventive measures and plan their long-term health strategy.
PCR testing for infectious diseases provides rapid and accurate identification of bacterial, viral, and fungal infections, including urinary tract infections, respiratory infections, and wound infections. Diagnostic PCR testing ensures timely treatment decisions and helps reduce the risk of complications.
Life Before Preventive Genomics
Ignoring health risks can escalate problems. Delayed diagnosis often leads to higher treatment costs, lifestyle limitations, long-term medication, and increased vulnerability for family members.
Genetic testing through NGS helps detect carriers of hereditary conditions, allowing individuals and families to understand their inherited risks and take proactive measures for long-term health.
Infectious disease PCR testing provides clinically validated, symptom-driven diagnosis, ensuring that infections are detected accurately and treated promptly. Early identification of pathogens supports better health outcomes and reduces the risk of severe complications.
