![]() ![]() Cataplexy is pathognomonic for narcolepsy and is present in around 70% of narcolepsy patients. Cataplexy attacks can last just a few seconds or many minutes. The emotional stimulus may be, for example, laughter, pleasure, anger or excitement. Ĭataplexy is defined as a sudden loss of voluntary muscle tone, with preserved consciousness, triggered by emotion. Autonomic symptoms have been reported in narcoleptic patients and include pupillary abnormalities, fainting spells, erectile dysfunction, night sweats, gastric problems, low body temperature, systemic hypotension, dry mouth, heart palpitations, headache and extremities dysthermia.EDS symptoms can severely disrupt daily life.Automatism occurs in many narcolepsy patients - when affected by severe sleepiness, they may have episodes in which they appear to be awake but lack full awareness and may behave inappropriately at such times.Excessive fatigue is a common complaint and is described by those affected as being a different symptom to sleepiness.They may nap during normal activities such as eating and talking.Patients with narcolepsy have persistent sleepiness, which may be irresistible.EDS and cataplexy are the key diagnostic symptoms. However, many patients do not have all these features. There is a tetrad of classic narcolepsy symptoms: excessive daytime sleepiness (EDS), cataplexy, hypnagogic hallucinations and sleep paralysis. Cataplexy, sleep paralysis and hypnagogic hallucinations may be due to REM sleep intruding into wakefulness. Dysregulation of rapid eye movement (REM) sleep may be part of the mechanism people with narcolepsy may enter REM sleep more quickly than those without narcolepsy.Patients with narcolepsy usually have a total sleep time similar to that of non-narcoleptic patients but their sleep is fragmented, with night-time sleep loss and daytime naps.Analysis of the cases has found that genetic predisposition to narcolepsy explains some of the variability noted in different countries although the mechanism is not completely understood. This was linked to two pandemic 2009-10 H1N1 influenza vaccines. A sudden increase in narcolepsy in children was seen in Finland and other European countries in 2010.Possible triggers include head trauma, infection and change in sleep habits.Most cases are sporadic but a familial form occurs in a small proportion of narcolepsy patients.Narcolepsy is associated with a specific HLA allele, DQB1*0602.Possibly, immunological mechanisms may lead to loss of hypocretin. Narcolepsy may be caused by the loss of a relatively few neurons that are responsible for producing the neuropeptide hypocretin in the CNS. This is derived from the hypothalamus and is thought to be involved in sleep/wake cycles, food intake and pleasure-seeking behaviour. The peptide hypocretin (orexin) may be involved.The precise cause of narcolepsy is unknown both environmental and genetic factors may play a part: First-degree relatives are at increased risk of narcolepsy compared with the general population.It is possible that incidence statistics would increase if diagnostic features were recognised at an earlier age. One study found that narcolepsy with cataplexy was often linked to complex movement disorders. Less than 5% of narcolepsy with cataplexy occurs in children.A smaller number of narcolepsy cases presents at around 35 years. Age of onset is typically around adolescence.P atients with narcolepsy without cataplexy are thought to represent only 36% of all narcolepsy patients. The prevalence of narcolepsy type 1 is between 25 and 100 per 100,000 people.In about 10 percent of cases, narcolepsy runs in families. Less often, the cause of narcolepsy is an injury that damages the brain. Their immune system mistakenly turns against their body and attacks the brain cells that produce hypocretin. Some people experience hallucinations and sleep paralysis when they’re falling asleep or waking up.Ĭertain people with autoimmune disorders are more likely to get narcolepsy with cataplexy. The lack of hypocretin makes it hard for someone to stay awake during the day, blurring the line between wakefulness and sleep. That loss of muscle tone causes you to lose control over your body when you’re awake. ![]() It’s the same loss of muscle tone that naturally happens during rapid eye movement (REM) sleep. The loss of muscle tone, cataplexy, happens because sleep and wakefulness overlap in narcolepsy. ![]() When it’s in short supply, your brain has trouble regulating your sleep-wake cycles. ![]() This chemical, which is produced in a brain region called the hypothalamus, controls sleep and wakefulness. Low levels of the chemical hypocretin cause narcolepsy with cataplexy. Narcolepsy affects signals in your brain that are supposed to keep you awake. ![]()
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