When:
October 19, 2022 – October 21, 2022 all-day
2022-10-19T00:00:00+01:00
2022-10-22T00:00:00+01:00
Where:
Conference Centre, The Royal College of Physicians of Edinburgh
9 Queen St
Edinburgh EH2 1JQ
UK
Conference on Alternating Hemiplegia of Childhood and ATP1A3 diseases @ Conference Centre, The Royal College of Physicians of Edinburgh | Scotland | United Kingdom

‘DEFINING THE FUTURE FOR AHC & ATP1A3 DISEASES’

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A 3 DAY UNIQUE EVENT INCORPORATING:

• 10-year anniversary conference commemorating the discovery of the ATP1A3 gene in AHC and ATP1A3 diseases

• The 10th Symposium on ATP1A3 in disease

This 3 Day unique event will be focused on those most impacted by research outcomes; with an opportunity to learn from their experiences and their priorities for future research to improve the research landscape and clinical care.

It will also include an overview of the last 10 years since the gene discovery, alongside current and future research plans for AHC and ATP1A3 Diseases.

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Where? – Hybrid event – EDINBURGH and ONLINE

Face-toFace VENUE:

Conference Centre, The Royal College of Physicians of Edinburgh,

9 Queens Street, Edinburgh, EH2 1JQ

 

When? – 19th-21st October 2022

The conference will run from Wednesday-Friday (programme to be released shortly), with an evening formal dinner for delegates and speakers on Thursday 20th October (Great Hall, The Royal College of Physicians of Edinburgh)

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BRINGING TOGETHER PEOPLE WITH LIVED EXPERIENCE OF

AHC AND ATP1A3 DISEASES, RESEARCHERS AND CLINICIANS

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To submit an oral or poster presentation, please email: support@ahcuk.org by 31st August 2022. All submissions must use accessible language and style. Prizes for best oral and poster presentation.

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The co-applicants and organising committee of the 10-year conference and 10th Symposium on ATP1A3 in disease are grateful for the generous grant from the European Joint Programme on Rare Diseases to support this event.