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A Murine Model of Dengue Virus-induced Acute Viral Encephalitis-like Disease
Published on: April 28, 2019
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[Bickerstaff brainstem encephalitis after upper respiratory infection].
Linda J Locht1, Morten Blaabjerg
1linda.Locht@rsyd.dk.
Ugeskrift for Laeger
|July 14, 2016
Summary
Bickerstaff brainstem encephalitis (BE) is a rare neurological disorder. This case highlights a probable BE diagnosis in a patient lacking anti-GQ1b antibodies, challenging typical diagnostic criteria.
Area of Science:
- Neurology
- Immunology
Background:
- Bickerstaff brainstem encephalitis (BE) is a rare neurological disorder characterized by ophthalmoplegia, ataxia, and altered sensorium, often following an infection.
- BE is typically associated with the anti-GQ1b antibody syndrome, placing it within the spectrum of Miller Fisher syndrome and Guillain-Barré syndrome.
Observation:
- This report details a 48-year-old woman presenting with symptoms consistent with probable BE.
- The patient's presentation occurred without the presence of anti-GQ1b antibodies.
Findings:
- The case provides a detailed account of the patient's history, diagnostic workup, treatment, and follow-up.
- The findings are analyzed in the context of international diagnostic criteria for BE.
Implications:
- This case expands the understanding of BE, particularly in presentations that deviate from the typical anti-GQ1b antibody association.
- It underscores the importance of considering BE even in the absence of specific antibodies, prompting a review of diagnostic guidelines.
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