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Case Reports: Rare disease
Late-onset multiple acyl-CoA dehydrogenase deficiency: an insidious presentation

Authors

  • Naini Nishita Rao Department of Endocrinology and Diabetes, Royal Perth Hospital, Perth, Western Australia, AustraliaSchool of Medicine, The University of Western Australia, Perth, Western Australia, Australia PubMed articlesGoogle scholar articles
  • Kharis Burns Department of Endocrinology and Diabetes, Royal Perth Hospital, Perth, Western Australia, AustraliaSchool of Medicine, The University of Western Australia, Perth, Western Australia, Australia PubMed articlesGoogle scholar articles
  • Catherine Manolikos Department of Endocrinology and Diabetes, Royal Perth Hospital, Perth, Western Australia, AustraliaDepartment of Dietetics and Nutrition, Royal Perth Hospital, Perth, Western Australia, Australia PubMed articlesGoogle scholar articles
  • Samantha Hodge Department of Endocrinology and Diabetes, Royal Perth Hospital, Perth, Western Australia, AustraliaDepartment of Dietetics and Nutrition, Royal Perth Hospital, Perth, Western Australia, Australia PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Naini Nishita Rao; n.nishita.rao{at}gmail.com
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Citation

Rao NN, Burns K, Manolikos C, et al
Late-onset multiple acyl-CoA dehydrogenase deficiency: an insidious presentation
BMJ Case Reports CP 2023;16:e252668.

Publication history

  • Accepted May 4, 2023
  • First published May 22, 2023.
Online issue publication 
January 24, 2024

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© BMJ Publishing Group Limited 2023. No commercial re-use. See rights and permissions. Published by BMJ.