Genomics Are a Lifesaver for Patients With Rare Diseases
In 2016, Jessica Wright became one of the first children to be diagnosed by the 100,000 Genomes Project, a program that provides whole-genome sequencing services for patients. She suffered from an unknown disease that caused epilepsy and affected her motor control. No treatment seemed to work. After years of numerous medical tests—from MRI scans to […]
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