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2 articles matching "genetics"

ResearchPUBMEDApr 1

Expanding Access to Genome Sequencing: Higher Diagnostic Yield in Self-Referred Participants From the CincyKidsSeq Study and Implications for Hybrid Models of Genetic Service Delivery.

Researchers tested whether people could get genetic testing (genome sequencing) without always needing to see a genetics specialist first. They studied 313 people of all ages who had unexplained symptoms and could refer themselves or be referred by any doctor. The study found that people who referred themselves were just as likely to get a diagnosis as those referred by specialists. This suggests a new way to make genetic testing available to more people while still having genetics experts review the results.

WHY IT MATTERSIf this hybrid model works, patients with rare diseases could access genome sequencing faster and more easily without waiting for a genetics specialist appointment, potentially shortening the diagnostic odyssey that many rare disease patients experience.
💬 Ask your doctorrare genetic diseasesundiagnosed genetic conditionsRead →
ResearchPUBMEDMar 26

[New ways in interdisciplinarity: internal medicine meets human genetics : When frequent conditions become rare and rare conditions become frequent].

Doctors are learning that common diseases are actually made up of many different rare subtypes when scientists look at their genetic makeup. By understanding the specific genetic changes in each person's disease, doctors can create targeted treatments that work better. This article uses chronic myeloid leukemia as an example—a treatment that targets one specific genetic change has turned a deadly disease into one people can live with for decades.

WHY IT MATTERSIf you have been diagnosed with a common cancer or disease, genetic testing may reveal you have a rare molecular subtype that qualifies you for a precision medicine treatment not available to patients with other genetic variations of the same disease.
💬 Ask your doctorchronic myeloid leukemiacancerRead →

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