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Case ReportsCase Report
Open Access

Post COVID-19 Guillain–Barre syndrome presents as sensory dominant neuropathy with reversible conduction failure

Abdulrahman M. AlTahan, Mohammed H. AlAnazi, Faisal A. AlTahan and Fatima A. AlAbandi
Neurosciences Journal January 2023, 28 (1) 57-61; DOI: https://doi.org/10.17712/nsj.2023.1.20220057
Abdulrahman M. AlTahan
From the Department of Medicine (AlAnazi), King Khalid University Hospital, from Department of Medicine (AlTahan), Dallah Hospital, from College of Medicine (AlTahan), King Saud University, Riyadh, Kingdom of Saudi Arabia, and from Royal College of Surgeons of Ireland (AlAbadani), Dublin, Ireland
MD, FRCP (London), FAAN
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  • For correspondence: [email protected]
Mohammed H. AlAnazi
From the Department of Medicine (AlAnazi), King Khalid University Hospital, from Department of Medicine (AlTahan), Dallah Hospital, from College of Medicine (AlTahan), King Saud University, Riyadh, Kingdom of Saudi Arabia, and from Royal College of Surgeons of Ireland (AlAbadani), Dublin, Ireland
MD, FRCP (Canada)
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Faisal A. AlTahan
From the Department of Medicine (AlAnazi), King Khalid University Hospital, from Department of Medicine (AlTahan), Dallah Hospital, from College of Medicine (AlTahan), King Saud University, Riyadh, Kingdom of Saudi Arabia, and from Royal College of Surgeons of Ireland (AlAbadani), Dublin, Ireland
MD
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Fatima A. AlAbandi
From the Department of Medicine (AlAnazi), King Khalid University Hospital, from Department of Medicine (AlTahan), Dallah Hospital, from College of Medicine (AlTahan), King Saud University, Riyadh, Kingdom of Saudi Arabia, and from Royal College of Surgeons of Ireland (AlAbadani), Dublin, Ireland
MB BCh BAO LRCP & SI
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Abstract

Guillain–Barré syndrome (GBS) has several clinical variants. The sensory presentations of GBS are atypical but well-recognized. We report a patient who presented with predominantly sensory symptoms associated with reversible conduction failure (RCF). RCF is a well-defined neurophysiological abnormality noted mainly in axonal GBS and may be misinterpreted as evidence of demyelination. A 25-year-old woman presented 2 weeks after a coronavirus 2019 infection with acute sensory symptoms, distal allodynia, mild weakness, and mild hyporeflexia in her upper limbs. A nerve conduction study (NCS) showed delayed motor distal latencies, and lumbar puncture confirmed cytoalbuminologic dissociation. After excluding other etiologies, she was diagnosed with GBS, treated with an IV immunoglobulin course, and showed remarkable recovery. Results of a repeat NCS were consistent with RCF and confirmed the presence of axonal GBS. Increased awareness of sensory GBS and RCF is expected to improve the diagnosis and management of atypical GBS presentations.

  • Received May 24, 2022.
  • Accepted October 26, 2022.
  • Copyright: © Neurosciences

Neurosciences is an Open Access journal and articles published are distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC). Readers may copy, distribute, and display the work for non-commercial purposes with the proper citation of the original work.

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Neurosciences Journal: 28 (1)
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Vol. 28, Issue 1
1 Jan 2023
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Post COVID-19 Guillain–Barre syndrome presents as sensory dominant neuropathy with reversible conduction failure
Abdulrahman M. AlTahan, Mohammed H. AlAnazi, Faisal A. AlTahan, Fatima A. AlAbandi
Neurosciences Journal Jan 2023, 28 (1) 57-61; DOI: 10.17712/nsj.2023.1.20220057

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Post COVID-19 Guillain–Barre syndrome presents as sensory dominant neuropathy with reversible conduction failure
Abdulrahman M. AlTahan, Mohammed H. AlAnazi, Faisal A. AlTahan, Fatima A. AlAbandi
Neurosciences Journal Jan 2023, 28 (1) 57-61; DOI: 10.17712/nsj.2023.1.20220057
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© 2025 Neurosciences Journal Neurosciences is copyright under the Berne Convention and the International Copyright Convention. All rights reserved. Neurosciences is an Open Access journal and articles published are distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC). Readers may copy, distribute, and display the work for non-commercial purposes with the proper citation of the original work. Electronic ISSN 1658-3183. Print ISSN 1319-6138.

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