Skip to content
| Home | Central Nervous System | Aromatic L-amino acid decarboxylase (AADC) deficiency | Congress activities International Symposium on Genetic Syndromes with Movement Disorders and Epilepsy (GSMDE)
International Symposium on Genetic Syndromes with Movement Disorders and Epilepsy (GSMDE)
The International Symposium on Genetic Syndromes with Movement Disorders and Epilepsy (GSMDE) was first held in February 2020, as a continuation of the International Symposium on Child Movement Disorders meetings.
Please select the resource of interest below:
View this infographic distributed at the
GSMDE Symposium 2020
which outlines the clinical diagnostics tests for, and the management of,
GSMDE brings experts in pediatric movement disorders together from across the world. Access PTC abstracts, presentations, posters, symposia and infographics from PTC activities at the symposium.
MED-ALL-AADC-2200032 | November 2022
Sign in or register to access exclusive content on this site
Close Register here to access the content on the site MED-ALL-CORP-2200029 | December 2022
You are now leaving MEDhub, a website provided by PTC Therapeutics. This link will take you to a website to which our
Privacy Statement and our Terms and Conditions do not apply.
MED-ALL-CORP-2200029 | December 2022
Close COMING SOON
The content you are trying to access is not currently available.
We will be updating the MEDhub site regularly to provide you with up-to-date, insightful expert-led content. To be notified when new additions become available,