Abstract
Kleine-Levin syndrome (KLS) is a rare, homogeneous, debilitating sleep disorder characterized by episodic hypersomnia, cognitive impairment, and behavioral changes. The etiology, pathophysiology, and optimal management of KLS remain uncertain. We identify the 5 key areas requiring urgent attention: KLS immunopathogenesis studies, next-generation genetics, multimodal functional imaging, biomarker discovery, and clinical drug trials. A centralized registry of afflicted individuals must be established. Disease uniformity should make the identification of associated genetic or imaging biomarkers easier, but clinical efforts require laboratory-based research to model the disease and generate preclinical data for clinical translation.
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Al Suwayri, S. M., & BaHammam, A. S. (2017, September 1). The “Known Unknowns” of Kleine-Levin Syndrome: A Review and Future Prospects. Sleep Medicine Clinics. W.B. Saunders. https://doi.org/10.1016/j.jsmc.2017.03.012
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