Performance of routine tasks without awareness.
Sudden and brief loss of muscle tone, often triggered by strong emotions or certain situations. Narcolepsy with cataplexy is known as narcolepsy type 1.
Complete collapse to the ground; all skeletal muscles are involved.
Only certain muscle groups are involved.
Biological clock mechanism that regulates the 24-hour cycle in the physiological processes of living beings. It is controlled in part by the SCN in the hypothalamus and is affected by the daily light-dark cycle.
Frequent awakenings and inappropriate transitions between states of sleep and wakefulness during nighttime sleep.
The inability to stay awake and alert during the day.
A neurotransmitter in the brain that supports wakefulness.
Vivid, realistic, and frightening dream-like events that occur when falling asleep.
A neuropeptide that supports wakefulness and helps suppress non-REM sleep and REM sleep.
Primary brain region for regulating the timing of sleep-wake states.
Unintentionally falling asleep due to excessive daytime sleepiness. Also known as “sleep attacks.”
Brief, unintentional lapses into sleep, or loss of awareness.
A validated objective measure of the tendency to fall asleep in quiet situations.
People with narcolepsy type 1 have low levels of hypocretin.
Narcolepsy without cataplexy; the cause of narcolepsy type 2 is unknown.
A state of sleep characterized by slower-frequency, more synchronized neuronal activity and decreased muscle tone. Deep stages help to restore the body.
A multiparameter test that monitors physiologic signals during sleep; used as a diagnostic tool in sleep medicine.
A state of sleep characterized by low-amplitude, fast-frequency EEG, vivid dreams, and loss of muscle tone. Normally occurs 60-90 minutes after sleep onset. Also known as “paradoxical sleep.”
Brief loss of control of voluntary muscles with retained awareness at sleep-wake transitions.
Sleep-onset REM period.