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Current insights in ultra-rare adenylosuccinate synthetase 1 myopathy – meeting report on the First Clinical and Scientific Conference. 3 June 2024, National Centre for Advancing Translational Science, Rockville, Maryland, the United States of America

Authors :
Emma Rybalka
Hyung Jun Park
Atchayaram Nalini
Dipti Baskar
Kiran Polavarapu
Hacer Durmus
Yang Xia
Linlin Wan
Perry B. Shieh
Behzad Moghadaszadeh
Alan H. Beggs
David L. Mack
Alec S. T. Smith
Wendy Hanna-Rose
Hyder A. Jinnah
Cara A. Timpani
Min Shen
Jaymin Upadhyay
Jeffrey J. Brault
Matthew D. Hall
Naveen Baweja
Priyanka Kakkar
Source :
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-18 (2024)
Publication Year :
2024
Publisher :
BMC, 2024.

Abstract

Highlights The inaugural Clinical and Scientific Conference on Adenylosuccinate Synthetase 1 (ADSS1) myopathy was held on June 3, 2024, at the National Institutes of Health (NIH) National Center for Advancing Translational Sciences (NCATS) in Rockville, Maryland, USA. ADSS1 myopathy is an ultra-rare, inherited neuromuscular disease. Features of geographical patient clusters in South Korea, Japan, India and the United States of America were characterised and discussed. Pre-clinical animal and cell-based models were discussed, providing unique insight into disease pathogenesis. The biochemical pathogenesis was discussed, and potential therapeutic targets identified. Potential clinical and pre-clinical biomarkers were discussed. An ADSS1 myopathy consortium was established and a roadmap for therapeutic development created.

Details

Language :
English
ISSN :
17501172
Volume :
19
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Orphanet Journal of Rare Diseases
Publication Type :
Academic Journal
Accession number :
edsdoj.0dfb7f65052b4eb2a4a20ba5da9a4309
Document Type :
article
Full Text :
https://doi.org/10.1186/s13023-024-03429-x