Integrate genomics seamlessly. Really.

Imagine knowing that a child is at risk for a rare disease and initiating a treatment plan before symptoms arise. Nurture Genomics expands upon current newborn screening with genomic sequencing for medically actionable, genetic disorders, early—when intervention matters most.

Integrate genomics seamlessly. Really.

Imagine knowing that a child is at risk for a rare disease and initiating a treatment plan before symptoms arise. Nurture Genomics expands upon current newborn screening with genomic sequencing for medically actionable, genetic disorders, early—when intervention matters most.

Actionable Genetic Conditions

WHAT IS NURTURE?

The Test: Whole genome sequencing to screen for 400+ actionable conditions + processing by a CLIA/CAP accredited lab associated with Harvard & MIT

The Support: Genetic counseling & care plans for parents and providers + peer-to-peer consults

The Future: Continued access to a child’s genomic profile

WHAT IS NURTURE?

The Test: Whole genome sequencing to screen for 400+ actionable conditions + processing a CLIA/CAP accredited lab associated with Harvard & MIT

The Support: Genetic counseling & care plans for parents and providers + peer-to-peer consults

The Future: Continued access to a child’s genomic profile

Actionable Genetic Conditions

WHY IT MATTERS

Too many children go
undiagnosed for too long.

70 percent
of rare genetic diseases start in childhood1.

5+ years
is the average time it takes to receive a rare disease diagnosis2.

We make it easy to integrate Nurture into your practice. Nurture manages the ordering, sequencing, analyzing, and interpretation so you can focus on patient care. With Nurture you’ll receive:

Clear, evidence-based insights and recommendations

Peer-to-peer consults with our expert medical team of genetic counselors, clinical geneticists, and physicians

Guidance for condition specific next steps

WHY IT MATTERS

Too many children go undiagnosed for too long.

70 percent
of rare genetic diseases start in childhood1.

5+ years
is the average time it takes to receive a rare disease diagnosis2.

Nurture manages the ordering, sequencing, analyzing, and interpretation so you can focus on patient care. With Nurture you’ll receive:

Clear, evidence-based insights and recommendations

Peer-to-peer consults with our expert medical team of genetic counselors, clinical geneticists

Guidance for condition specific next steps

Play Video

What Families Learn

Know more about Nurture and the genomic health insights we provide to our members.

Play Video

What Families Learn

Know more about Nurture and the genomic health insights we provide to our members.

Together, let’s help families take charge of the process, find answers early and get the support they need to access the best care possible.

Together, let’s help families take charge of the process, find answers early and get the support they need to access the best care possible.

Let's Collaborate

We’d love to discuss your questions and provide more detailed information.

CONTACT:
Molly OShea, MD, FAAP

molly@nurturegenomics.com
Pediatric Medical Director, Nurture Genomics
Pediatrician owner, Birmingham Pediatrics + Wellness Center, Bloomfield Hills, MI

LEARN MORE ABOUT OUR PHYSICIAN NETWORK

Let's Collaborate

We’d love to discuss your questions and provide more detailed information.

CONTACT:
Molly OShea, MD, FAAP

molly@nurturegenomics.com
Pediatric Medical Director, Nurture Genomics
Pediatrician owner, Birmingham Pediatrics + Wellness Center, Bloomfield Hills, MI

© Copyright 2024 Nurture Genomics, All Rights Reserved

© Copyright 2024 Nuture Genomics
All Rights Reserved