Recurrent rhabdomyolysis and an autosomal dominant family history of scoliosis: clinical features leading to a diagnosis of metabolic myopathy

Authors

  • Dr. Sarah L. Wright, FRACP, PhD 1 Department of Neurology, University College London Hospitals NHS Foundation Trust, London, UK https://orcid.org/0000-0002-1146-1801
  • Dr. Stefen Brady, FRCP, DPhil Department of Neurology, Oxford University Hospitals NHS Foundation Trust, Neurology, Oxford, Oxfordshire, UK

DOI:

https://doi.org/10.17161/rrnmf.v3i3.16318

Keywords:

RYR1, Scoliosis, Rhabdomyolysis

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Published

2022-09-26

Issue

Vol. 3 No. 3 (2022)

Section

Clinic and Case Reports

License

Copyright (c) 2022 Sarah L. Wright FRACP PhD, Stefen Brady FRCP DPhil

Creative Commons License

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

How to Cite

Wright, S., & Brady, S. (2022). Recurrent rhabdomyolysis and an autosomal dominant family history of scoliosis: clinical features leading to a diagnosis of metabolic myopathy. RRNMF Neuromuscular Journal, 3(3), 10. https://doi.org/10.17161/rrnmf.v3i3.16318