3D-GATA2 Consortium Members Present at the 11th EWOG-MDS/SAA International Symposium
November 10, 2025
The 3D GATA2 consortium has launched a survey to understand better the experiences, needs, and perspectives of people living with GATA2 deficiency and their families.
We invite people living with GATA2 deficiency, caregivers of someone with GATA2 deficiency, and family members of someone who was affected by GATA2 deficiency to take part in the survey.
Why is this survey important?
GATA2 deficiency is a rare genetic condition with a wide range of clinical manifestations. Although research is advancing our understanding of the condition, many aspects of its natural course remain unknown.
The 3D GATA2 research project brings together a large European clinical network to study GATA2-deficient patients and improve our understanding of the disease. By combining clinical and scientific research with the experiences and perspectives of patients and families, the project aims to contribute to a more complete understanding of GATA2 deficiency and, ultimately, support more personalised care for affected individuals.
The patient and family perspective is an essential part of this work.
Through this survey, we want to learn more about the experiences of people affected by GATA2 deficiency, the challenges they face, and their needs and priorities. The responses will help ensure that the patient and family perspective is taken into account in current and future research on GATA2 deficiency.
Who can take part?
The survey is open to:
- People living with GATA2 deficiency
- Caregivers of someone with GATA2 deficiency
- Family members of someone who was affected by GATA2 deficiency
📅 Open until 31 October 2026
🌍 Available in English, French, German, Dutch, Spanish, Italian and Portuguese