RARE and undiagnosed

https://editions.rarerevolutionmagazine.com/html5/reader/production/default.aspx?pubname=&edid=5fddfc62-9dc6-47bf-aa6a-922d41bce312&pnum=44 For families living with ring 20 chromosome syndrome, diagnosis offers few answers and little relief. With science unable to reveal the genomic change behind the syndrome’s symptoms, patients endure a trial-and-error approach to care. Founder Allison Watson and the Ring20 Research and Support charity are championing a future where a true diagnosis and targeted therapies can one day transform care for this ultra-rare condition.