Orphanet Journal of Rare Diseases (Nov 2024)

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

  • 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

DOI
https://doi.org/10.1186/s13023-024-03429-x
Journal volume & issue
Vol. 19, no. 1
pp. 1 – 18

Abstract

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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.

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