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Letter
Acetazolamide can improve symptoms and signs in ion channel-related congenital myopathy

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Footnotes

  • Contributors EM: drafting the manuscript for content, analysis or interpretation of data, study concept. LH: revising the manuscript for content, analysis or interpretation of data, study concept. RS: revising the manuscript for content, analysis or interpretation of data. MGH: revising the manuscript for content, analysis or interpretation of data. FM: revising the manuscript for content, analysis or interpretation of data, study concept. PM: revising the manuscript for content, analysis or interpretation of data, study concept.

  • Funding EM has received funding from an NIHR rare disease TRC postdoctoral fellowship, which is supported via the UCLH NIHR BRC. Part of this work was undertaken at University College London Hospitals/University College London, which received a proportion of funding from the Department of Health’s National Institute for Health Research Biomedical Research Centres funding scheme. MGH is supported by a Medical Research Council Centre grant, the UCLH NIHR BRC and receives research funding from the Muscular Dystrophy Campaign. FM is supported by the National Institute for Health Research Biomedical Research Centre at Great Ormond Street Hospital for Children NHS Foundation Trust and University College London.

  • Competing interests None declared.

  • Patient consent Next of kin consent obtained.

  • Ethics approval The London—West London and GTAC Research Ethics Committee.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Data sharing statement This is a letter describing two clinical cases. All data are reported in the letter.

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