✨ Turner Syndrome Across the Lifespan: What We Know Now — and What’s Changing ✨

Join us on February 24th at 11:00 AM EST for an important global conversation on Turner syndrome.

We are honored to welcome Professor Claus Højbjerg Gravholt, who will share insights into how our understanding of Turner syndrome continues to evolve — from childhood through adulthood. This session will explore current knowledge, emerging perspectives, and what these developments may mean for individuals, families, and clinicians around the world.

Turner syndrome care is changing. Awareness is growing. Research is advancing.
Now is the time to stay informed.

🌍 Multiple time zones available
🕚 Live session begins at 11:00 AM EST

Whether you are a patient, parent, advocate, or healthcare professional, this is a conversation you won’t want to miss.

👉 Mark your calendar and join us on February 24th!

Overview

Join our FREE virtual event to discover new findings and practical recommendations to improve care for children with idiopathic short stature.

Join Us For The Redefining ISS: Improving Confidence and Clarity| Virtual Launch Event

Tuesday 27th January 2026: 8:30-9:30 PST | 9:30-10:30 MST | 10:30-11:30 CST | 11:30-12:30 EST | 13:30-14:30 BRT | 16:30 –17:30 GMT | 17:30 - 18:30 CET

REGISTER HERE: https://www.eventbrite.com/e/redefining-iss-improving-confidence-and-clarity-launch-event-tickets-1980649315420?aff=oddtdtcreator

Idiopathic short stature (ISS) refers to children who are significantly shorter than peers with no established cause. For many families, ISS affects far more than height – it can have a negative impact on children’s physical, emotional, and social wellbeing.

Families also experience inconsistent diagnostic experiences, delayed referrals, limited access to support, and uncertainty in care pathways. Our Redefining ISS project aims to change this.

This virtual event will showcase the findings of the Redefining ISS project, most importantly a set of implementable recommendations created by the group to improve both quality of life and care for children with ISS and their families. Further insights will be shared by a healthcare professional and we have invited a family to speak on their experiences with ISS.