What we screen for

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Your Child’s DNA Tells a Story.

Knowing that story can help you write their next chapter

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What we screen for

Autism & Neurodevelopmental Disorders

Cardiovascular

Dermatology

Ear, Nose, & Throat

Endocrinology

Gastroenterology

Hematology

Immunology

Malformations

Metabolic

Multi-system

Muscular

Neurology

Oncology

Ophthalmology

Respiratory

Urology

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.

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.

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.

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.

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.

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.

View a Comprehensive List

Insights That Grow With Your Child

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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Supporting All Stages of Development

Genomic Insights Across Childhood and Beyond

Genomic screening isn’t just 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.

Newborn

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

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

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

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

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

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

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

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

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

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.

Team Up With Your Pediatrician & Care Team.

We believe in teamwork when it comes to your child's health. Fore makes it easy to involve your pediatrician and care team every step of the way. You can seamlessly share your child’s genetic test results, giving their doctor an additional tool to personalize healthcare as your child grows.

Easily share digital results with your pediatrician

Use our secure platform to keep track of updates and follow-ups

Get real-time support from our network of licensed physicians and genetic counselors

Get ongoing, expert genetic counseling at your fingertips.

PGX Insights that look at your child’s DNA to determine how they might respond to certain medications. This information can help doctors choose the medicine and dose that’s most likely to work best for your child and avoid ones that might cause side effects.

CLIA-certified and CAP-accredited lab processing, military-grade encryption HIPAA-compliant data management ensure the safety and privacy of your information.

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Real families. Real results. Real peace of mind.

Explore how early genetic screening can save lives

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March 13, 2026|Matthew Pelo

Malignant Hyperthermia — A Life Saved on the Operating Table Note: Real cases, names and ages have been changed for privacy. The Family Anna and Mike opted for a Fore...

Henry's Story – A silent threat uncovered

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Dilated Cardiomyopathy Type 1G — A Silent Threat Uncovered Note: Real cases, names and ages have been changed for privacy. The Family Elena and Chris had a family history of...

Ava's Story – An infection prevented before it even started

March 13, 2026|Matthew Pelo

Sarah and Daniel were first-time parents to baby Noah. He seemed healthy at birth, but by four months old, he had already had two serious infections requiring hospitalization. They asked...

Maya's Story – A life saved on the operating table

March 13, 2026|Matthew Pelo

Malignant Hyperthermia — A Life Saved on the Operating Table Note: Real cases, names and ages have been changed for privacy. The Family Anna and Mike opted for a Fore...

Henry's Story – A silent threat uncovered

March 13, 2026|Matthew Pelo

Dilated Cardiomyopathy Type 1G — A Silent Threat Uncovered Note: Real cases, names and ages have been changed for privacy. The Family Elena and Chris had a family history of...

Ava's Story – An infection prevented before it even started

March 13, 2026|Matthew Pelo

Sarah and Daniel were first-time parents to baby Noah. He seemed healthy at birth, but by four months old, he had already had two serious infections requiring hospitalization. They asked...