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Autoinflammatory syndromes in neurology: when our first line of defence misbehaves
  1. William K Diprose1,2,
  2. Anthony Jordan3,
  3. Neil E Anderson1
  1. 1Department of Neurology, Auckland City Hospital, Auckland, New Zealand
  2. 2Department of Medicine, Faculty of Medical and Health Sciences, The University of Auckland, Auckland, New Zealand
  3. 3Department of Clinical Immunology and Allergy, Auckland City Hospital, Auckland, New Zealand
  1. Correspondence to Dr William K Diprose, Department of Neurology, Auckland City Hospital, Auckland 1023, New Zealand; william.diprose{at}auckland.ac.nz

Abstract

Autoinflammatory syndromes result from a defective innate immune system. They are characterised by unexplained fever and systemic inflammation involving the skin, muscle, joints, serosa and eyes, along with elevated acute phase reactants. Autoinflammatory syndromes are increasingly recognised as a cause of neurological disease with a diverse range of manifestations. Corticosteroids, colchicine and targeted therapies are effective if started early, and hence the importance of recognising these syndromes. Here, we review the neurological features of specific autoinflammatory syndromes and our approach (as adult neurologists) to their diagnosis.

  • neuroimmunology
  • immunology
  • rheumatology
  • clinical neurology
  • haematology

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Footnotes

  • Correction notice This article has been corrected since it was published Online First. The abstract has been modified slightly.

  • Contributors WKD was commissioned to write the article. AJ provided immunology expertise. NEA provided neuroimmunology expertise. All authors contributed to writing and approving the manuscript.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests None declared.

  • Provenance and peer review Commissioned. Externally peer reviewed by Neil Scolding, Bristol, UK.

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