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CSF1 receptor-related leukoencephalopathy
  1. Ikechukwu Chukwuocha1,
  2. Simon Ubben2,
  3. Mary O'Driscoll3,
  4. Alison Seymour4
  1. 1Neurology, Royal Wolverhampton Hospitals NHS Trust, Wolverhampton, UK
  2. 2Neurology, New Cross Hospital, Wolverhampton, UK
  3. 3Clinical Genetics, Birmingham Women's and Children's NHS Foundation Trust, Birmingham, UK
  4. 4Rehabilitation Medicine, West Park Hospital, Wolverhampton, UK
  1. Correspondence to Dr Ikechukwu Chukwuocha, Neurology, Royal Wolverhampton Hospitals NHS Trust, Wolverhampton, UK; ikechukwu.chukwuocha{at}nhs.net

Abstract

A 51-year-old woman developed subacute progressive gait and cognitive difficulties, with depression and anxiety. She had psychomotor slowing, axial rigidity, fixed dystonic posturing of right hand and symmetrical generalised bradykinesia. MR brain scan identified bilateral multifocal non-enhancing high signal intensity in the frontal subcortical and periventricular areas, with corpus callosal thinning and areas of paraventricular diffusion restriction, suggesting an adult-onset leukodystrophy. Genetic analysis identified a heterogenous pathogenic variant in the colony-stimulating factor 1 receptor (CSF1R) causing this autosomal dominant leukoencephalopathy (OMIM 221820). The patient was unusual in having a CSF1R-related leukoencephalopathy without a relevant family history.

  • NEUROGENETICS
  • NEUROPSYCHIATRY
  • NEUROPATHOLOGY

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Data availability statement

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Footnotes

  • Collaborators Not applicable.

  • Contributors All authors were involved in the conceptualisation, design and revision of the manuscript. SU is the guarantor.

  • 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 Not commissioned; externally peer reviewed by David Lynch, London, UK.

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