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.

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What We Test For

When you understand your child’s genetic makeup, you’re no longer left guessing about their health. You gain the clarity to act early, prevent what’s preventable, and support their well-being at every stage of life.

Brain & Developmental Conditions

Identify conditions linked to learning, motor skills, and communication.

Heart Health

Detect hidden heart rhythm or structural risks before symptoms appear.

Growth & Metabolism

Find conditions that affect how the body uses food and energy.

Cancer Risk

Spot genetic changes that may increase the chance of certain cancers.

Inherited Conditions

Reveal genetic traits passed down in families that could impact your child’s health.

Medication Response

Understand how your child’s body might react to common medicines, helping doctors choose the safest, most effective options.

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Key Stages of Life

Select the Key Stages

Newborn
Infant
Toddler
Child
Teen

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.

Real Families. Real Results. Real Peace of Mind.

Explore how early genetic screening can save lives

An infection prevented before it even started

Read Ava's story

A silent threat uncovered

Read Henry's story

A life saved on the operating table

Read Maya's story
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