What is KLS ?
KLS is a rare disorder characterised by recurrent episodes of excessive sleep, associated with reduced understanding and altered behaviour. KLS usually starts in the teenage years, but can occur in younger children and adults.
Each episode can last days, weeks or months. Individuals in episode are often not able to care for themselves, attend school or go to work. Between episodes they go back to being themselves with normal sleep, understanding and behaviour.
It can be difficult to diagnose and treat but the impact on young people and their families is devastating.
What are the main symptoms of KLS?
Symptoms vary between individuals with KLS but the following three symptoms have to be present in an episode for a diagnosis;
Excessive Sleep
Excessive Prolonged Sleep (Hypersomnia). Sleep 15 to 22 hours for days, weeks or even months.
Learn MoreCognitive Impairment
Confusion, Reduced understanding, feel in a dreamlike state (derealisation).
Learn MoreAltered Behaviour
Behaviour becomes childlike or different to normal, apathetic and uncommunicative.
Learn MoreOther common symptoms during episode may include changed eating habits, irritable when prevented from sleeping, disinhibited behaviour (swearing, hypersexuality), migraines, hallucinations, anxiety. Some have little or no memory of events after an episode.
As KLS is a syndrome, symptoms vary between individuals and episodes.
Our Mission & Goals
KLS Support UK is a small charity that supports families affected by Kleine-Levin Syndrome, raises awareness and supports research.
Awareness
Raise awareness of KLS in the UK amongst the medical profession and the general public.
Learn moreMedical Research
Support medical research with the aim of finding the cause, treatment and ultimately a cure for KLS.
Learn moreWork with other Groups
Co-operate with other KLS groups around the world to further these aims.
Learn moreLatest News
Recent Posts
Trustee meeting today!
- Planning a Family Day on September 11th 2022, venue being organised ..
- New website being launched soon ….
— KLS Support UK (@KLSSupportUK) June 1, 2022
Trustee meeting today!
- Planning a Family Day on September 11th 2022, venue being organised ..
- New website being launched soon ….
Research in Kleine-Levin syndrome is extremely limited. Really happy to see this paper out, and for UK patients to have made a contribution to this study, identifying possible genetic factors leading to KLShttps://t.co/q3pfDmYTJb
— Guy Leschziner (@guy_lesch) March 18, 2021
Research in Kleine-Levin syndrome is extremely limited. Really happy to see this paper out, and for UK patients to have made a contribution to this study, identifying possible genetic factors leading to KLShttps://t.co/q3pfDmYTJb
— Guy Leschziner (@guy_lesch) March 18, 2021@AtrialHypati The Royal Free Hospital HYPTIA team rocks!
@AtrialHypati The Royal Free Hospital HYPTIA team rocks!







