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Published on: September 20, 2024
Acute encephalitis induced Kleine-Levin syndrome with episodic vertical gaze dysfunction during hypersomnia episodes
Hui Lv1, Xiaoyan Long1, Yefan Lv1
1Department of Neurology, Xiangya Hospital, Central South University, Jiangxi, China.
Abstract:
Kleine-Levin syndrome (KLS) is a rare, recurring sleep disorder that easily ignored. Episodic upward-gaze palsy is an uncommon manifestation observed in patients of KLS, which further complicates this disorder. Although peripheral microbial infection have been recognized as most common triggers for KLS, the underlying pathophysiology of this disorder remains unclear. We reported a unique case of KLS elicited by acute encephalitis, which was confirmed by pleocytosis of cerebrospinal fluid at the early stage. The cerebrospinal fluid returned to normal over time while the attacks continued to recur frequently. Episodic upward-gaze palsy was observed during attacks and clinical symptoms were exacerbated following a subsequent COVID-19 infection. This report presents a classic KLS case with distinctive characteristics, which should facilitate more accurate and earlier diagnosis for clinicians. Furthermore, it provides a new perspective for understanding the pathogenesis of this rare disease.
Citation:
Lv H, Long X, Lv Y, Zhou J. Acute encephalitis induced Kleine-Levin syndrome with episodic vertical gaze dysfunction during hypersomnia episodes. J Clin Sleep Med. 2024;20(9):1555-1556.
Insights
Kleine-Levin syndrome (KLS), a rare sleep disorder, can be triggered by acute encephalitis. This case highlights episodic upward-gaze palsy and symptom exacerbation after COVID-19, offering new insights into KLS.
Area of Science:
- Neurology
- Sleep Medicine
- Infectious Disease
Background:
- Kleine-Levin syndrome (KLS) is a rare, recurrent sleep disorder.
- Episodic upward-gaze palsy is an uncommon KLS manifestation.
- Pathophysiology of KLS remains unclear, though infections are common triggers.
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