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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 Workshop is intended to provide a forum for collaborative continuous clinical education and interdisciplinary networking as well as an introduction to novel diagnostic methods and translational research on rare congenital skeletal disorders. The number of participants is limited to 70. The official language is English. Register on website, no later than January 31.
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