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GeneDx Holdings Corp.: GeneDx Presents New Data at the American Epilepsy Society Annual Meeting Demonstrating That Exome Sequencing Outperforms Multi-Gene Panels for Patients with Epilepsy

GeneDx Holdings Corp.: GeneDx Presents New Data at the American Epilepsy Society Annual Meeting Demonstrating That Exome Sequencing Outperforms Multi-Gene Panels for Patients with Epilepsy
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Broader test gives hope to millions of newborns

CINCINNATI — Brynn Schulte nearly died twice when she was a baby, at one point needing emergency surgery for massive bleeding in her brain. ....

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Genetic test breakthrough offers hope to millions of babies | National & World News

Tests for sick newborns that look at their full genetic blueprints are nearly twice as good at finding genetic problems as narrower, more commonly used tests, a recent study found. According to the research, published in the Journal of the American Medical Association, the broader tests found 49% of genetic abnormalities, compared with 27% for the narrower tests. Experts say this offers hope to parents of millions of babies with confounding conditions.

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Tufts Medical Center , United States , Rhode Island , Sleeping Beauty , Paul Kruszka , Lindsay Schulte , Mike Schulte , Amanda Denaro , Philip Brooks , Jon Davis , Cristina Tarango , Jill Maron , Brynn Schulte , Mara Aspinall , National Institutes Of Health , Journal Of The American Medical Association , Cincinnati Children Hospital Medical Center , Arizona State University , Us National Human Genome Research Institute , American Medical , Human Genome Research Institute , Cincinnati Children , Hospital Medical Center , Infants Hospital , Cash Denaro , National Institutes ,

Genetic test breakthrough offers hope to millions of babies

Tests for sick newborns that look at their full genetic blueprints are nearly twice as good at finding genetic problems as narrower, more commonly used tests, a recent study found. According to the research, published in the Journal of the American Medical Association, the broader tests found 49% of genetic abnormalities, compared with 27% for the narrower tests. Experts say this offers hope to parents of millions of babies with confounding conditions.

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A broad genetic test could help millions of newborns

Brynn Schulte nearly died twice when she was a baby, at one point needing emergency surgery for massive bleeding in her brain. No one knew what was wrong until a test that looked at her full genetic blueprint found a rare bleeding disorder called factor XIII deficiency. ....

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