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Pediatric Medical Genetics

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Caring for Kids with Complex Genetic Disorders

The pediatric medical geneticists at Cedars‑Sinai Guerin Children’s understand that it can feel overwhelming to learn your child might have a genetic condition. It’s why we specialize in hard-to-diagnose conditions and leave no stone unturned when it comes to getting you the answers your family deserves.

  • Experts in Rare Conditions

    We have the expertise to diagnose rare and ultra-rare disorders as well as common pediatric conditions. Our team can help you find the right care for your child.

  • Fast, Accurate Testing

    We work with the best laboratories and research partners to provide our patients with comprehensive molecular testing for the most accurate diagnosis.

  • Family‑Based Approach

    Testing the whole family helps identify inherited or new conditions and provides you with a roadmap for long-term care and treatments.

Areas of Expertise

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Locations

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Innovators in Pediatric Medical Genetics

Researchers and doctors at Cedars‑Sinai helped establish the field of medical genetics. That pioneering spirit continues to this day as we help patients and families understand genetic disorders, manage conditions and find the most effective treatments. 

Medical Genetics News From Guerin Children’s

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Essential Reference Outlines Deformations and How to Treat Them

A new edition of the defining reference guide on deformations and birth defects outlines the latest clinical guidance.

Answers for Children With Angelman Syndrome

Angelman syndrome, a rare neurodevelopmental condition with symptoms similar to autism, is misdiagnosed in half of all children with the condition.

Do Children Need Genetic Testing?

Learn how working with a medical geneticist can uncover genetic conditions in children and guide treatment decisions.

3D Cameras Could Help Diagnose Rare Genetic Diseases

Many rare genetic disorders are difficult to diagnose in infants and children, except through costly DNA tests. A Cedars-Sinai investigator is leveraging an unexpected instrument...

Marathon Baby

Fueled by the power of knowledge and unparalleled access to supportive resources, Matt and Marci Tatham take their young son’s genetic disorder, Klinefelter syndrome, in...

Translational Genetic Research

Our physicians and doctors work in relentless pursuit of the right test for the right patient at the right time. Whether that’s discovering new techniques for rapid genomic sequencing or developing novel 3D facial‑recognition technology, we are committed to helping patients live their best lives. 

Genomics Core

The Genomics Core gathers and translates genome, transcriptome, epigenome and metagenome information for clinical and basic research.

Cytogenetics Lab

This lab uses specialized techniques to evaluate congenital and acquired chromosome abnormalities.

Researcher in lab
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