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Survey about achondroplasia
We have designed a questionnaire with the purpose to better know the population connected to achondroplasia.
The questionnaire is optional and anonymous. The data obtained will be used for statistical purposes and to better understand the natural history of achondroplasia. Please consider answering.
If you would like to take the survey later, you can click on the link at the top "Register at BA"

The EAF (European Achondroplasia Forum) is a network of specialists in achondroplasia representative of the achondroplasia clinical community.

Ahead of The EAF upcoming workshop on 27th October, 16:30 CET, Clinical Management Challenges in Infants and Young Children with Achondroplasia, the network is undertaking two surveys to establish the challenges of managing achondroplasia in these age groups: one for parents of children with achondroplasia and one for clinicians.


The results will form the starting point for discussions at the workshop, which aims to compare follow-up recommendations with each person's reality, identifying barriers to best practices and launching the debate on how to overcome them. The parent survey is available in English, French, German, Italian, Spanish and Portuguese.

Deadline for participating in the questionnaire: 3 October 2022

Workshop: Clinical Management Challenges In Infants And Young Children With Achondroplasia

27 October 2022 | 16:30 (CET)


The workshop is online, free of charge, and open to participation by anyone. Inês Alves, founder of Beyond Achondroplasia, will be speaking. To register click on the button below:

eaf programme
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