S•H•A•R•E® - Support, Help and Resources for Epilepsy

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Epilepsy is a brain disorder where clusters of cells in the brain called neurons send abnormal signals. It's these abnormal brain signals that make people with epilepsy prone to seizures.1 There are many types of seizures and they can vary from brief disruptions of the senses, to short periods of unconsciousness, to convulsions.

It is important to note that all people with epilepsy will have seizures, but all people with seizures will not necessarily be diagnosed with epilepsy.

Epileptic seizures are typically classified into categories:

Partial seizures originate in a specific part of the brain, and include:

Generalized seizures involve the entire brain, and include:

Unclassified epileptic seizures

Infantile spasms are a specific type of seizure seen in an epilepsy syndrome of infancy and childhood also known as West Syndrome


Partial seizures

Partial seizures start in a specific area of the brain and are categorized by whether or not the person loses consciousness.2

  • Simple partial seizures do not involve a loss of consciousness. Symptoms vary depending on the area of the brain involved in the seizure, but may include muscle contractions or twitching, numbness and tingling in body parts, hallucinations, a feeling of déjà vu, jerky motions, or weakness of a body part. Simple partial seizures usually last less than 2 minutes.2,3
  • Complex partial seizures impair consciousness, where the person is unable to respond to commands, interact with their surroundings, or recall events that occurred during the seizure. This seizure type originates in one particular area of the brain and can produce motor and behavioral disturbances. As a complex partial seizure begins, the person may present with a blank or wide-eyed stare followed by such activities as chewing, lip smacking, picking at their shirt, or other repetitive, purposeless movements. Typically, complex partial seizures last between 30 and 90 seconds, and are often followed by a period of disorientation, confusion and/or fatigue.3,4,5
  • Secondarily generalized seizures are partial seizures that have spread to other regions of the brain. Complex partial seizures that evolve to secondarily generalized seizures last no more than a few minutes, are difficult to distinguish from primary generalized seizures, and are more likely to manifest as a tonic-clonic seizure.3

Generalized seizures

In contrast to partial seizures, generalized seizures involve both sides of the brain at once.

  • Absence (Petit mal) seizures are brief seizures usually lasting 5 to 15 seconds. Petit mal seizures involve sudden, brief impairment of consciousness, including a blank stare with motor or behavioral disturbances. These seizures frequently begin in childhood and may persist into adulthood. If untreated, these seizures may occur multiple times per day.3
  • Myoclonic seizures are rapid, brief episodes of alternating contractions and relaxations (jerking or twitching) of a muscle or a group of muscles. Myoclonic seizures usually cause abnormal movements on both sides of the body at the same time.4
  • Clonic seizures appear as repetitive jerking movements or contractions of a group of muscles. The arms, neck and facial muscles are involved. The movements cannot be stopped by restraining or repositioning the arms or legs. Clonic seizures vary in length between 1 to 2 minutes.3,4,5
  • Tonic seizures involve sudden stiffening of the muscles. Tonic seizures most often occur during sleep and usually involve all or most of the brain, affecting both sides of the body. During a tonic seizure, the person will usually remain conscious, and the seizure will usually last less than 20 seconds.4
  • Tonic-clonic (grand mal) seizures combine the characteristics of both tonic and clonic seizures. They may begin with loss of consciousness and stiffening of the body or extremities (tonic phase) followed by jerky movements (clonic phase). The seizure may last 1 or 2 minutes and is often associated with loss of control of the bladder or bowels. Patients look cyanotic (blue), salivate profusely, and bite their tongues. In the period following the seizure, the person may experience stupor, sleepiness, confusion, headache, and muscle soreness.3
  • Atonic seizures occur when the muscles suddenly lose strength. The eyelids may droop, the head may nod, and the person may drop things and often falls to the ground. These seizures are also called "drop attacks" or "drop seizures." The person usually remains conscious and the seizures generally last less than 15 seconds.4

Unclassified seizures

Some seizures do not easily fit into the abovementioned categories. These seizures are referred to as unclassified. This group also includes those seizures with an unclear nature.3


Infantile spasms

Infantile spasms are clusters of brief seizures appearing in the first year of life. During these spasms, the child may suddenly bend forward, stiffen his or her body, arms and legs, or arch his or her torso. A child may experience dozens of these clusters of spasms each day. An individual spasm typically lasts for less than one second, but may last up to 5 seconds. Infants may have dozens of clusters and several hundred spasms per day.6


References:

  1. National Institute of Neurological Disorders and Stroke. NINDS Epilepsy Information page. Available at: http://www.ninds.nih.gov/disorders/epilepsy/epilepsy.htm. Updated July 2, 2008. Accessed July 14, 2008.
  2. Foldvary-Schaefer N, Wyllie E. Epilepsy. In: Goetz CG. Textbook of Clinical Neurology. 3rd ed. Philadelphia, PA: WB Saunders; 2007.
  3. Sadler RM. Epilepsy and Seizures. In: Noble J, et al, eds. Textbook of Primary Care Medicine. 3rd ed. St.Louis, MO: Mosby; 2001.
  4. Epilepsy.com. Available at: http://www.epilepsy.com. Accessed February 25, 2008.
  5. Aminoff MJ. Electrophysiology. In: Goetz CG. Textbook of Clinical Neurology. 3rd ed. Philadelphia, PA: WB Saunders; 2007.
  6. National Institute of Neurological Disorders and Stroke. NINDS Infantile Spasms Information Page. http://www.ninds.nih.gov/disorders/infantilespasms/infantilespasms.htm. Last accessed 08/6/2009.

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