Literature DB >> 31982280

PRES-like presentation in MOG antibody-related demyelination (MARD).

Joel Corbett1, Sandeep Bhuta2, Kerri Prain3, Fabienne Brilot4, Arman Sabet5, Simon A Broadley5.   

Abstract

A 33-year-old male presented with a progressive four-week history of frontal headache and left visual field impairment. MRI brain confirmed bilateral, asymmetric, occipital vasogenic oedema, suggestive of posterior reversible encephalopathy syndrome (PRES). Serum testing for MOG antibodies was positive, confirming a diagnosis of MOG antibody-related demyelination (MARD). A similar PRES-like pattern of white matter inflammation has been reported previously in neuromyelitis optica spectrum disorder but has not previously been reported in MARD. Crown
Copyright © 2020. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Myelin oligodendrocyte glycoprotein; Posterior reversible encephalopathy syndrome

Mesh:

Substances:

Year:  2020        PMID: 31982280     DOI: 10.1016/j.jocn.2020.01.034

Source DB:  PubMed          Journal:  J Clin Neurosci        ISSN: 0967-5868            Impact factor:   1.961


  2 in total

1.  Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease Presenting as Intracranial Hypertension: A Case Report.

Authors:  Jaydip Ray Chaudhuri; Jui Jade Bagul; Alluri Swathi; Bhim Sen Singhal; N Chakradhar Reddy; Kiran Kumar Vallam
Journal:  Neurol Neuroimmunol Neuroinflamm       Date:  2022-10-19

Review 2.  Magnetic resonance imaging in neuromyelitis optica spectrum disorder.

Authors:  Laura Clarke; Simon Arnett; Kate Lilley; Jacky Liao; Sandeep Bhuta; Simon A Broadley
Journal:  Clin Exp Immunol       Date:  2021-07-06       Impact factor: 4.330

  2 in total

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