(See also Overview of Movement and Cerebellar Disorders Overview of Movement and Cerebellar Disorders Voluntary movement requires complex interaction of the corticospinal (pyramidal) tracts, basal ganglia, and cerebellum (the center for motor coordination) to ensure smooth, purposeful movement... read more .)
Classification of myoclonus
Myoclonus may be classified as physiologic (benign) or pathologic (1 Classification reference Myoclonus is a brief, shocklike contraction of a muscle or group of muscles. Diagnosis is clinical and sometimes confirmed by electromyographic testing. Treatment includes correction of reversible... read more ).
Physiologic myoclonus may occur when a person is falling asleep and during early sleep phases (called hypnic myoclonus). Hypnic myoclonus can be focal, multifocal, segmental, or generalized (see below) and may resemble a startle reaction. Another type of physiologic myoclonus is hiccuping (diaphragmatic myoclonus).
Other causes of pathologic myoclonus include degenerative disorders affecting the basal ganglia and some dementias.
Myoclonus may also be classified as follows:
By its distribution: Focal, segmental (contiguous areas), multifocal (noncontiguous areas), or generalized
By its site of origin: Cortical, subcortical, segmental, or peripheral
By clinical presentation: Positive or negative
By its etiology: Essential (primary), acquired, or idiopathic
By its trigger: Sensory or spontaneous
Myoclonus classified by site of origin is as follows:
Cortical: Cortical myoclonus is associated with cerebral cortex damage or epilepsy. Photic visual stimuli or touching may trigger myoclonic jerks, which may cause abnormalities on an electroencephalogram (eg, focal or generalized spike-and-wave or polyspike-and-wave epileptiform discharges, giant somatosensory evoked potentials). The myoclonic jerks may be less evident at rest but aggravated during motor action. This type of myoclonus can severely impair speech and gait.
Subcortical: Subcortical myoclonus is associated with disorders that affect the basal ganglia or other subcortical structures. Its effects are similar to those of cortical myoclonus. However, there are no electroencephalogram abnormalities or giant somatosensory evoked potentials, and photic visual stimuli are not a trigger. The category of subcortical myoclonus includes essential myoclonus, myoclonus-dystonia, reticular reflex myoclonus, startle syndromes, Creutzfeldt–Jakob disease Creutzfeldt-Jakob Disease (CJD) Creutzfeldt-Jakob disease (CJD) is the most common human prion disease. It occurs worldwide and has several forms and subtypes. CJD symptoms include dementia, myoclonus, and other central nervous... read more , and subacute sclerosing panencephalitis Subacute Sclerosing Panencephalitis (SSPE) Subacute sclerosing panencephalitis is a progressive, usually fatal brain disorder occurring months to usually years after an attack of measles. It causes mental deterioration, myoclonic jerks... read more (1 Classification reference Myoclonus is a brief, shocklike contraction of a muscle or group of muscles. Diagnosis is clinical and sometimes confirmed by electromyographic testing. Treatment includes correction of reversible... read more ).
Segmental and peripheral: Forms of segmental or peripheral myoclonus are relatively rare. Segmental myoclonus includes spinal segmental and propriospinal myoclonus. Spinal segmental myoclonus refers to myoclonus in spinal muscles of one or several contiguous segments of the spinal cord. Propriospinal myoclonus is characterized by slowly propagated movements that spare the face, often with a burst duration incompatible with other types of myoclonus. Palatal myoclonus, now mainly considered a misnomer, has been reclassified as palatal tremor. The most common peripheral myoclonus is hemifacial spasm Hemifacial Spasm Hemifacial spasm refers to unilateral painless, synchronous contractions of facial muscles due to repetitive involuntary electrical impulses from the 7th cranial (facial) nerve and/or its motor... read more ; it results primarily from vascular compression of the facial nerve as it exits from the brain stem or from compression by cerebellopontine angle tumors. Hemimasticatory spasm is much rarer; it is characterized by unilateral, paroxysmal contractions of the jaw muscles. It may be caused by compression of the motor branch of the trigeminal nerve.
Classifying myoclonus based on site of origin is thought to be the most helpful when choosing the most effective treatment.
Clinical presentation of patients with myoclonus may be classified as positive or negative:
Positive: Patients have an active muscle twitch leading to a jerk.
Negative: Muscle tone suddenly lapses (with electrographic silence on electromyography); when antigravity muscles lose muscle tone, the patient may fall. Negative myoclonus includes asterixis (eg, flapping of the hands that occurs in patients with severe liver failure).
Positive and negative myoclonus often occur in the same patient.
Etiology of myoclonus may be essential (primary), acquired (most common), or idiopathic.
Essential (primary) myoclonus has no identifiable cause and/or is suspected to involve genetic factors.
Idiopathic myoclonus is myoclonus whose presence is completely unexplained.
Myoclonus may have a trigger or not:
Sensory sensitive: Myoclonus is triggered by a stimulus (eg, sudden noise, movement, light, visual threat), as can occur when a person is suddenly startled (startle response).
Spontaneous: Myoclonus occurs without a trigger, as often occurs when the cause is metabolic.
Symptoms and Signs of Myoclonus
Myoclonus can vary in amplitude, frequency, and distribution.
Muscle jerks may occur spontaneously or be induced by a stimulus (eg, sudden noise, movement, light, visual threat).
Myoclonus that occurs when patients are suddenly startled (startle myoclonus) may be an early symptom of Creutzfeldt-Jacob disease. Creutzfeldt-Jakob Disease (CJD) Creutzfeldt-Jakob disease (CJD) is the most common human prion disease. It occurs worldwide and has several forms and subtypes. CJD symptoms include dementia, myoclonus, and other central nervous... read more
Myoclonus due to severe closed head trauma or hypoxic-ischemic brain damage may worsen with purposeful movements (action myoclonus) or may occur spontaneously when movement is limited because of injury.
Myoclonus due to metabolic disturbances may be multifocal, asymmetric, and stimulus-induced; it usually involves facial or proximal limb muscles. If the disturbance persists, generalized myoclonic jerks and, ultimately, seizures may occur.
Diagnosis of Myoclonus
Diagnosis of myoclonus is clinical. Testing is done based on clinically suspected causes. Brain imaging is done.
Treatment of Myoclonus
Correcting the metabolic disturbance or other cause if possible
Stopping or reducing the dose of the causative drug
Drug therapy to relieve symptoms
Treatment of myoclonus begins with correction of underlying metabolic disturbances or other causes if correctable. If a drug is the cause, the drug is stopped, or the dose is reduced.
For symptom relief, clonazepam 0.5 to 2 mg orally 3 times a day is often effective. Valproate 250 to 500 mg orally 2 times a day or levetiracetam 250 to 500 mg orally 1 or 2 times a day may be effective; rarely, other antiseizure drugs help. Doses of clonazepam or valproate may need to be lower in older patients.
Site of origin for myoclonus can help guide treatment. For example, valproate, levetiracetam, and piracetam tend to be effective in cortical myoclonus but ineffective in other types of myoclonus. Clonazepam may be effective in all types of myoclonus. In some cases, a combination of drugs is necessary.
In the past, many types of myoclonus seemed to respond to the serotonin precursor 5-hydroxytryptophan, which was used with the oral decarboxylase inhibitor carbidopa, but 5-hydroxytryptophan is not used anymore because better drugs are now available.
Myoclonus is a brief, shocklike muscle contraction that can vary in severity and distribution.
Myoclonus can be physiologic (eg, hiccuping, sleep-related muscle contractions) or secondary to various brain disorders, systemic disorders, or drugs.
If a metabolic disturbance is the cause, correct it, and when necessary, give drugs (eg, clonazepam, valproate, levetiracetam) to relieve symptoms.