The gender incongruence module in the European Registries for Rare Endocrine & Bone Conditions (EuRREB): first results, current insights, and future directions
The data collected so far highlight the importance of wide multicenter data collection in advancing knowledge on the care of TGD adolescents. Expanding this registry and fostering international collaboration will be crucial in standardizing protocols, improving care, and guiding evidence-based recommendations for TGD youth.
Authors
- Daniel Klink
- Sabine E Hannema (ORCID: https://orcid.org/0000-0002-8996-0993)
- Silvia Ciancia (ORCID: https://orcid.org/0000-0003-0874-4648)
- S. Faisal Ahmed (ORCID: https://orcid.org/0000-0003-0689-5549)
- Kanetee Busiah (ORCID: https://orcid.org/0000-0002-1059-0791)
- М. С. Черенько (ORCID: https://orcid.org/0000-0003-1731-2994)
- Hedi L. Claahsen‐van der Grinten (ORCID: https://orcid.org/0000-0003-0181-0403)
- Aneta Gawlik-Starzyk
- Martine Cools (ORCID: https://orcid.org/0000-0002-9552-4899)
- Wiktoria Kempińska
Institutions
- Radboud University Nijmegen (NL)
- Medical University of Silesia (PL)
- Leiden University Medical Center (NL)
- Ghent University Hospital (BE)
- Radboud University Medical Center (NL)
- Amalia Kinderziekenhuis (NL)
- University of Glasgow (GB)
- Vrije Universiteit Amsterdam (NL)
- University of Lausanne (CH)
Publication Details
- Journal
- Endocrine Connections
- Published
- 2025-10-01
- DOI
- https://doi.org/10.1530/ec-25-0401
- Primary Topic
- LGBTQ Health, Identity, and Policy
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Fonds Wetenschappelijk Onderzoek
- Universiteit Gent
- Vlaamse regering