Newly Diagnosed?

If you’re here because your child or loved one has just received a Kleefstra syndrome (KS) diagnosis, please know this: you are not alone. We understand how overwhelming, emotional, and confusing this moment can feel—and we want you to take a deep breath. You’ve found a community that not only shares your journey, but walks it together with compassion, information, and hope.

Welcome to your Family by Fate.

What is Kleefstra syndrome (KS)?

Kleefstra syndrome (KS) is a rare genetic disorder characterized by intellectual disability, childhood hypotonia, severe expressive speech delay and a distinctive facial appearance with a spectrum of additional clinical features. The syndrome, eponymously named for Dr. Tjitske Kleefstra, is caused by either a mutation or deletion of a gene called EHMT1 (Euchromatic Histone Methyltransferase 1). The impact leads to the loss of the entire gene.

Kleefstra Syndrome presents with a wide range of symptoms, and the severity of those symptoms vary from mild to severe.

Join the IDefine + Kleefstra Syndrome Community on Social Media

 Wherever you are in your journey, connect, share, and learn through our social platforms below.

Facebook

Facebook

Follow Us
Instagram

Instagram

Follow Us
LinkedIn

LinkedIn

Connect
YouTube

YouTube

Subscribe

You Belong Here. Get Engaged with the Community.

Whether your journey has just begun or you’re still searching for answers, IDefine is here to walk with you. We believe that empowered families drive progress—and we’re committed to providing support, advocacy, and the resources you need every step of the way.

If you have questions or need help getting started, please don’t hesitate to contact us directly. We’re here for you.

Connect

with a parent

Join

 the Rare-X Data
Collection effort

Receive

 the latest news

Accelerate

drug
development

Kleefstra Clinic at the Rosamund Stone Zander Translational Neuroscience Center

Resources

Follow IDefine and sign up for our newsletter to stay on top of all our news, announcements and community interest stories.

Kleefstra Syndrome Facebook Pages

We are a global community! There are support groups set up as private, closed groups on Facebook for various regions around the world. 

Global Genes

Global Genes is a global non-profit advocacy organization for individuals and families fighting rare and genetic diseases.

National Organization for Rare Diseases (NORD)

NORD is a patient advocacy organization dedicated to individuals with rare diseases and the organizations that serve them. NORD’s Resource Center provides patients and caregivers with free webinars, fact sheets, infographics and other helpful materials to guide you on your journey with a rare disease.

Have a resource to suggest?
Please email us at unlock@idefine.org
Thank you!

As IDefine continues working towards our mission, we are seeking partners and volunteers who can help us raise funds and organize our efforts to build this much needed resource for the Kleefstra Syndrome community. If you would like to donate time, talent and resources to further our mission, we would love to hear from you.

Please reach out at Unlock@IDefine.org
Our Current Needs:

– IT Coordinator
– Development Director
– Data Management Coordinator
– Communications Team Member
– Fundraising Team Member

We would love to hear from you.

If you have any questions feel free to contact us. We will be sure to get back to you as soon as possible.