Genomic Insights Across Childhood and Beyond

Genomic screening isn’t a one-time test — it’s a lifelong tool that evolves with your child. From birth through adulthood, genetic insights shape personalized care, enable early interventions, and provide ongoing guidance for better health outcomes.

What We Test For

Brain & Developmental Conditions

Learn about rare genetic syndromes that can affect how your baby’s brain develops—impacting motor skills, learning, or behavior. Early support can make a huge difference in your child’s future.

Heart Health Risks

Some children are born with hidden heart conditions that may not show symptoms until it's too late. We screen for genetic markers linked to heart rhythm issues or structural problems—so your pediatrician can take steps early.

Growth & Nutrition Challenges (Metabolic)

Metabolic disorders affect how your child processes food and energy. Left untreated, they can impact growth and brain development. Catching them early means avoiding serious complications.

Early Cancer Risk Detection

Some cancers can run in families—even in childhood. We check for inherited risks for rare pediatric cancers, so you can watch for early signs and follow the best prevention plan.

Family-Inherited Conditions

If a condition runs in your family, your child might be at risk too. Our screen identifies these inherited genetic variants to help your doctor create a care plan just for your child.

Medication Safety & Response

Every child’s body responds to medications differently. We include results from FDA-recognized pediatric pharmacogenomic guidelines—so doctors can prescribe safer, more effective medications if your child ever needs them.

Key Stages of Life

One test will provide information….

Select the Key Stages

Newborn

Why it matters: Early detection of genetic conditions can dramatically improve health outcomes. Identifying risks at birth enables immediate, sometimes life-saving interventions.

Examples of impact:

Inborn errors of metabolism (e.g., PKU, galactosemia): Early treatment prevents severe complications.
Cystic fibrosis: Diagnosis at birth enables specialized care from day one.
Congenital heart defects: Genomic insight can support early detection and timely surgery.
Rare conditions: Screening may reveal hard-to-diagnose conditions not caught by standard newborn screening.

Infant

Why it matters: As your baby grows, some genetic conditions begin to appear. Early identification leads to more effective treatments and better long-term outcomes.

Examples of impact:

Muscular dystrophies (e.g., Duchenne): Early diagnosis allows for proactive care and symptom management.
Immunodeficiency disorders: Enables proactive care to prevent life-threatening infections.
Metabolic disorders: Ongoing monitoring supports optimal nutrition and growth.
Spinal muscular atrophy (SMA): Early treatment can preserve motor function.

Toddler

Why it matters: Genomic screening can help explain or anticipate developmental concerns, enabling personalized care during this critical period.

Examples of impact:

Neurodevelopmental disorders (e.g., autism): Early diagnosis unlocks early intervention.
Hematological disorders (e.g., sickle cell disease): Enables tailored care plans.
Genetic predispositions: Early awareness of future risks (e.g., cancer or heart disease).
Developmental delays: Genetic insights can guide targeted therapies.

Child

Why it matters: Continued genomic insights can guide your child’s health journey — from managing emerging conditions to customizing care.

Examples of impact:

Neurological conditions (e.g., epilepsy, ADHD): Enables precise diagnosis and treatment.
Endocrine disorders (e.g., type 1 diabetes, thyroid disease): Early detection improves management.
Medication response (pharmacogenomics): Choosing the right medication, the first time.

Teen

Why it matters: As your child matures, genomic screening supports proactive decisions — from preventive care to reproductive health.

Examples of impact:

Cardiovascular disease (e.g., familial hypercholesterolemia): Enables early lifestyle or medical intervention.
Cancer risks: Awareness can guide screenings and prevention.
Medication response (pharmacogenomics): Reduces trial and error with prescriptions.
Reproductive planning: Understand inherited risks before starting a family.