Causes of narcolepsy
The causes remain unknown. A genetic component is known to exist, but the possibility that the cause is an autoimmune reaction is gaining increasing support.
Narcolepsy is a chronic disorder of sleep–wake regulation. It may cause excessive sleepiness and involuntary sleep episodes, even after a night of sleep.
Type 1 is associated with cataplexy and/or low hypocretin (orexin). Type 2 does not involve cataplexy. Distinguishing them requires a specialist assessment.
The causes remain unknown. A genetic component is known to exist, but the possibility that the cause is an autoimmune reaction is gaining increasing support.
The main characteristic is excessive daytime sleepiness and a feeling of constant tiredness, with sudden, uncontrollable sleep attacks in any place and situation.
We must distinguish two types of narcolepsy: type 1 and type 2. Type 1 features an absence of hypocretin in the cerebrospinal fluid. Type 2 maintains hypocretin levels and does not involve cataplexy.
Sleepiness is the core symptom. Other manifestations vary, and their absence does not rule out narcolepsy. A single symptom is not enough to establish a diagnosis.
A difficult-to-control need to sleep and involuntary sleep episodes. These can affect education, work and daily activities.
Brief muscle weakness triggered by laughter or another emotion: knees may buckle, the head may drop or the jaw may slacken, without losing consciousness.
When waking up or falling asleep, a person may be aware but temporarily unable to move. This can also occur without narcolepsy.
Vivid images, sounds or sensations may occur when falling asleep or waking up. On their own, these do not mean a psychiatric disorder.
Despite marked daytime sleepiness, nights may include repeated awakenings. Falling asleep easily by day does not necessarily mean sleeping well at night.