ReNU Syndrome

Variants in RNU4-2 Uncovered as One of the Most Prevalent Causes of Rare Neurodevelopmental Disorders

Discovery Renews Hope for Affected Families Worldwide

“It is remarkable that around 100,000 individuals globally who are predicted to have ReNU syndrome have DNA changes in just 13 of the over 3 billion base-pairs of our genetic code!”

Map

Have a diagnosis? There’s strength in numbers! Share your rare by adding a ReNU family member to the map or gallery.

ReNU Hope Conference

Attend or support the Inaugural ReNU Hope Family Conference and Scientific Symposium!

Research

Data collection programs may enable us to accelerate research and the development of new drugs, devices, or other therapies.

More Information

Learn about how ReNU occurs, typical features and characteristics, how development is affected, and why this was only recently discovered!

Parent Connection

You’re not alone! ‘ReNU’ hope and find community with ReNU Syndrome parents worldwide that understand and relate to your experience.

Donations

Promoting more research, building community, and spreading awareness...there's still lots to learn and the sky is the limit!