The Test: Whole genome sequencing for 400+ actionable, childhood-onset genetic conditions
A better approach to better health.
Genomic screening for early detection and action.
A better approach to better health.
Genomic screening for early detection and action.
Rethinking “rare” disease.
With more than 6,000 rare diseases affecting over 20 million Americans, chances are you know someone with a rare disease.3.
80 percent
of rare diseases are genetic3.
1 out of every 2
people diagnosed with rare disease is a child4.
5+ years
is the average time it takes to receive a diagnosis5.
Early genomic screening in childhood can transform the way rare genetic conditions are managed and have a profound and lasting impact on health.
Rethinking
“rare” disease.
With more than 6,000 rare diseases affecting over 20 million Americans, chances are you know someone with a rare disease.3.
80 percent
of rare diseases are genetic3.
1 out of every 2
people diagnosed with rare disease is a child4.
5+ years
is the average time it takes to receive a diagnosis5.
Early genomic screening in childhood can transform the way rare genetic conditions are managed and have a profound and lasting impact on health.
WHAT IS NURTURE?
More than just a test.
Too often, genetic conditions in children are misdiagnosed or diagnosed late, costing precious time for effective treatment. Nurture combines comprehensive genomic sequencing and support to identify conditions early — when intervention matters most — and offers a clear view of the road ahead.
The Support: Genetic counseling + care plans + accelerated access to specialists
The Future: Ongoing support for a year + continued access to your child’s genomic profile
WHAT IS NURTURE?
More than
just a test.
Too often, genetic conditions in children are misdiagnosed or diagnosed late, costing precious time for effective treatment. Nurture combines comprehensive genomic sequencing and support to identify conditions early — when intervention matters most — and offers a clear view of the road ahead.
The Test: Whole genome sequencing for 400+ actionable, childhood-onset genetic conditions
The Support: Genetic counseling + care plans + accelerated access to specialists
The Future: Ongoing support for a year + continued access to your child’s genomic profile
WHO CAN BENEFIT MOST FROM NURTURE?
Healthy kids in
early childhood
Symptoms for many genetic conditions may not manifest for weeks, months, or even years. Nurture screens for over 400 actionable conditions, empowering you to identify potential health risks and intervene proactively. The optimal window for screening is shortly after birth, but screening in later years can also be beneficial. If you have specific medical concerns, you should consult your pediatrician.
WHO CAN BENEFIT MOST FROM NURTURE?
Healthy kids in
early childhood
Symptoms for many genetic conditions may not manifest for weeks, months, or even years. Nurture screens for over 400 actionable conditions, empowering you to identify potential health risks and intervene proactively. The optimal window for screening is shortly after birth, but screening in later years can also be beneficial. If you have specific medical concerns, you should consult your pediatrician.
CARE NAVIGATION
Learning that your child is at increased risk for a genetic condition can be scary. That’s why Nurture stays at your side, helping you move forward with knowledge and confidence.
Learning that your child is at increased risk for a genetic condition can be scary. That’s why Nurture stays at your side, helping you move forward with knowledge and confidence.
Spotlight on:
Wilson’s Disease
Wilson's Disease is one of the 413 genetic conditions Nurture screens for. This genetic disorder prevents the body from removing copper and can be a progressive form of liver failure. Wilson's Disease affects one out of every 30,000 infants. It is difficult to diagnose, but easy to treat when identified early.
Knowledge = Power.
Early knowledge = Priceless.
Challenging to Diagnose
Wilson's disease is present at birth, but is unknown until copper builds up in the liver, brain, or other organs and initiates symptoms. Symptoms vary and can include fatigue, jaundice, and fluid buildup.
- Most people are diagnosed between 5 and 35 years old.
- Neurological complications may cause developmental delay.
- Liver transplant may be necessary.
Knowing early changes everything
- Genomic sequencing alerts you to the risk.
- Nurture provides you and your pediatrician with guidance.
- Nurture recommends specialists for care.
- Once diagnosed, the right treatment is initiated early.
- Developmental delay and transplant avoided.
Spotlight On:
Wilson’s Disease
Wilson's Disease is one of the 413 genetic conditions Nurture screens for. This genetic disorder prevents the body from removing copper and can be a progressive form of liver failure. Wilson's Disease affects one out of every 30,000 infants. It is difficult to diagnose, but easy to treat when identified early.
Knowledge = Power.
Early knowledge = Priceless.
Challenging to Diagnose
Wilson's disease is present at birth, but is unknown until copper builds up in the liver, brain, or other organs and initiates symptoms. Symptoms vary and can include fatigue, jaundice, and fluid buildup.
- Most people are diagnosed between 5 and 35 years old.
- Neurological complications may cause developmental delay.
- Liver transplant may be necessary.
Knowing early changes everything
- Genomic sequencing alerts you to the risk.
- Nurture provides you and your pediatrician with guidance.
- Nurture recommends specialists for care.
- Once diagnosed, the right treatment is initiated early.
- Developmental delay and transplant avoided.
