J Korean Neurol Assoc.  1999 Sep;17(5):705-709.

A Case of Kleine-Levin Syndrome

Affiliations
  • 1Department of Neurology, Seoul National University, College of Medicine.
  • 2Yonjung Brain Function & Sleep Research Center.

Abstract

Kleine-Levin syndrome (KLS) is a rare disorder and is diagnosed by recurrent episodes of hypersomnia, hyperphagia, and neurobehavioral dysfunctions. We present a case of a male 19 year-old with seven episodes of the above symptoms. All episodes occurred after a respiratory infectious illness and spontaneously resolved after a few days or a few weeks. A polysomnography showed prolonged sleep latency and decreased REM sleep (14.6%). A multiple sleep latency test revealed a slightly short mean sleep latency (8min 7sec) and three sleep-onset REM episodes in a series of four sleep latency tests across a one day period. The electrophysiological features of previously reported were reviewed.


MeSH Terms

Disorders of Excessive Somnolence
Humans
Hyperphagia
Kleine-Levin Syndrome*
Male
Polysomnography
Sleep, REM
Young Adult
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