Hunter syndrome is a lysosomal storage disorder caused by a deficiency in the enzyme iduronate-2-sulfatase (I2S). The disease was first described in 1917 by physician Charles A. Hunter (1873-1955), a ...

In many ways Ryan Austin is like any other 5-year-old. He loves to run and play with his mom and dad. However, when Ryan was only 2 his parents noticed something was different. They said he started to ...

When Melissa Hogan's son Case was 2, doctors diagnosed him with Hunter syndrome, a rare genetic disease with a terrible prognosis: children with Hunter syndrome gradually lose the ability to walk, ...

Last year, the Muedder family discovered that their then 2-year-old son Finn has Hunter syndrome, a rare genetic disease with a terrible prognosis — children with it slowly lose their ability to walk, ...

Emily Lieber is the kind of teacher you remember: Patient and fun, energetic and creative. Many of the kindergartners and first graders she has taught at Meredith Elementary School in South ...

DelveInsight’s, “Hunter Syndrome Pipeline Insight 2025” report provides comprehensive insights about 10+ companies and 10+ pipeline drugs in Hunter Syndrome pipeline landscape. It covers the pipeline ...

Denali Therapeutics shows promising early-phase data with DNL310 in Hunter syndrome, alongside robust Q2 financials, including $183.4M net income. Despite a strong cash position and revenue ...

It’s going to be a long wait, but RegenXBio is already waving a flag to show that the Hunter syndrome gene therapy RGX-121 is headed for an accelerated approval request at the FDA. The company has ...

Explore Hunter Syndrome causes, symptoms, diagnosis, treatment, and what to expect to better understand this rare inherited ...

The Lieber family, based in Roxborough, was recently presented the “Communications Champion Brighter Futures” award by Philadelphia’s Department of Behavior Health and Intellectual disABILITY Services ...

Hunter syndrome is an inherited disorder where glycosaminoglycans (GAGs) build up in cells of the body due to a deficiency of the enzyme iduronate-2-sulfatase. There is no cure for the syndrome and ...