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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 :
Rybalka, Emma
Park, Hyung Jun
Nalini, Atchayaram
Baskar, Dipti
Polavarapu, Kiran
Durmus, Hacer
Xia, Yang
Wan, Linlin
Shieh, Perry B.
Moghadaszadeh, Behzad
Beggs, Alan H.
Mack, David L.
Smith, Alec S. T.
Hanna-Rose, Wendy
Jinnah, Hyder A.
Timpani, Cara A.
Shen, Min
Upadhyay, Jaymin
Brault, Jeffrey J.
Hall, Matthew D.
Source :
Orphanet Journal of Rare Diseases. 11/26/2024, Vol. 19 Issue 1, p1-18. 18p.
Publication Year :
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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17501172
Volume :
19
Issue :
1
Database :
Academic Search Index
Journal :
Orphanet Journal of Rare Diseases
Publication Type :
Academic Journal
Accession number :
181133450
Full Text :
https://doi.org/10.1186/s13023-024-03429-x