IntellxxDNA genomic testing

Whereas genetics is the study of individual genes and their inheritance, genomics is the study of the entire genome.  Our genes are not our destiny.  There are many factors, such as environmental and lifestyles, that interact with our genome to turn things on or off (gene regulation).  

Genomics studies the complete set of DNA in an organism, known as the genome. It investigates genome structure, function, evolution, and mapping as well as gene-environment and gene-gene interactions. Genomics plays a critical role in understanding gene interactions, diagnosing genetic disorders, and advancing personalized medical treatments.

IntellxxDNA genomic testing examines known changes in the genome that may increase a person’s risk for certain conditions. It identifies genetic variations related to nutrients, inflammation, mitochondrial function, detoxification, immune function, brain structure (scaffolding), brain plasticity, and neurotransmitters, and provides research-based information to support interpretation and treatment planning. This approach may lead to more effective treatments with less trial and error.

For example, a person may have a gene variant associated with a higher risk of obsessive-compulsive disorder (OCD), but if they do not exhibit any signs or symptoms of OCD, that gene is unlikely to be playing a significant role. Conversely, if a person has severe OCD and also has gene variations associated with increased risk, those genes may be contributing factors to their current symptoms. Understanding the research-based evidence related to specific gene variations can help guide treatment decisions.

Getting genomic sequencing is an investment.  Although our understanding of these genes may change with time, our genes remain the same throughout our lifetime.  Deciding whether the cost is justified is a personal decision influenced by various factors. 

Many families with children on the autism spectrum invest significant amounts in tests, therapies, and treatments, often with varying degrees of success. Families dealing with PANDAS or PANS often face challenges in accessing effective treatments for their children, who might experience persistent or recurring symptoms. Families of children with ADHD sometimes spend substantial amounts monthly on stimulant medications. 

Evidence-based insights based on genetic variations into possible dietary adjustments, vitamins, supplements, lifestyle modifications, or medication choices, are expanding every year. Genomic testing, such as IntellxxDNA, can identify potential genetic contributors that may influence health.  By identifying potential genetic contributors that may influence health, we can leverage known data about those genes to help inform which dietary adjustments, vitamins, supplements, lifestyle modifications, and/or medications may benefit your child.

Precision medicine is a personalized approach to healthcare that customizes treatment based on an individual's unique characteristics, such as their genetic profile, lifestyle, and environmental factors. 

By utilizing genomic testing, precision medicine aims to uncover the specific causes of a disease in each person, allowing for the identification of the most effective treatments tailored to their unique needs.