#Narcolepsy cataplexy symptoms full

For example, using the Epworth Sleepiness Scale.

They are often visual but may be auditory, tactile or multisensory.ДЄ thorough history is important, with particular reference to:.

These occur at the onset of sleep (hypnagogic) or on awakening (hypnopompic).

It may be alarming and associated with a sensation of inability to breathe (although diaphragmatic breathing usually continues through the episodes).

It affects approximately one third of narcolepsy patients.

Patients are aware but are, briefly, unable to move or open their eyes.

This may occur as the patient is falling asleep or awakening.

The weakness is usually bilateral but one case report describes unilateral attacks.

Frequency varies, from several attacks per day to less than one per year.

Hearing, awareness and consciousness are intact.

Slurred speech and visual symptoms such as blurred vision or diplopia may be experienced.

In severe attacks, all voluntary muscles except the diaphragm may be affected.

Severity can vary - eg, from a barely susceptible slackening of the facial muscles, dropping of the jaw or the entire head, to weakness at the knees or collapse on to the floor.

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. Д¬ataplexy 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.

#Narcolepsy cataplexy symptoms full

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.