See also: Generalised epilepsy
Tonic–clonic seizure |
Classification and external resources |
ICD-10 |
G40.3 |
ICD-9 |
345.3 |
MedlinePlus |
000695 |
eMedicine |
neuro/376 |
MeSH |
D004830 |
Tonic–clonic seizures (formerly known as grand mal seizures) are a type of generalized seizure that affects the entire brain. Tonic–clonic seizures are the seizure type most commonly associated with epilepsy and seizures in general, though it is a misconception that they are the only type.
Tonic–clonic seizures are induced deliberately in electroconvulsive therapy.
Contents
- 1 Pathophysiology
- 2 Phases
- 3 See also
- 4 References
- 5 External links
Pathophysiology
The vast majority of generalized seizures are idiopathic.[1] However, some generalized seizures start as a smaller seizure such as a simple partial seizure or a complex partial seizure and then spread to both hemispheres of the brain. This is called a secondary generalization.[2] Factors could include chemical and neurotransmitter imbalances and a genetically determined seizure threshold, both of which have been implicated. The seizure threshold can be altered by fatigue, malnutrition, lack of sleep or rest, hypertension, stress, diabetes, the presence of neon or xenon strobe-flashes, fluorescent lighting, rapid motion or flight, blood sugar imbalances, anxiety, antihistamines and other factors.[3]
In the case of symptomatic epilepsy, it is often determined by MRI or other neuroimaging techniques that there is some degree of damage to a large number of neurons.[4] The lesions (i.e., scar tissue) caused by the loss of these neurons can result in groups of neurons episodically firing abnormally, creating a seizure.
Phases
The seizures are divided into two phases, the tonic phase and the clonic phase, hence the name of the seizure.
- Tonic phase
- The patient will quickly lose consciousness, and the skeletal muscles will suddenly tense, often causing the extremities to be pulled towards the body or rigidly pushed away from it, which will cause the patient to fall if standing or sitting. The tonic phase is usually the shortest part of the seizure, usually lasting only a few seconds. The patient may also express brief vocalizations like a loud moan or scream during the tonic stage, due to air forcefully expelled from the lungs.
- Clonic phase
- The patient's muscles will start to contract and relax rapidly, causing convulsions. These may range from exaggerated twitches of the limbs to violent shaking or vibrating of the stiffened extremities. The patient may roll and stretch as the seizure spreads. The eyes typically roll back or close and the tongue often suffers bruising or lacerations sustained by strong jaw contractions. The lips or extremities may turn slightly bluish (cyanosis) and incontinence is seen in some cases.
Due to physical and nervous exhaustion, postictal sleep with stertorous breathing invariably follows a tonic–clonic seizure. Confusion and complete amnesia upon regaining consciousness is usually experienced and slowly wears off as the patient becomes gradually aware that a seizure occurred.
See also
- Epileptic seizure and Non-epileptic seizure
- Absence seizure
- Seizures Associated with LGS
- Seizures associated with Lennox-Gastaut syndrome (LGS)
References
- ^ David Y Ko (5 April 2007). "Tonic–Clonic Seizures". eMedicine. Retrieved 2008-03-19.
- ^ "Epilepsy Action: Simple Partial Seizures". Epilepsy Action. British Epilepsy Association. 19 February 2008. Retrieved 2008-03-19.
- ^ "Seizure Mechanisms and Threshold". Epilepsy Foundation. Retrieved 2008-03-19.
- ^ Ruben Kuzniecky, M.D. (16 April 2004). "Looking at the Brain". epilepsy.com. Epilepsy Therapy Project. Retrieved 2008-03-19.
External links
- Tonic–clonic seizure at DMOZ
Seizures and epilepsy (G40–G41, 345)
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Basics |
- Seizure types
- Aura (warning sign)
- Postictal state
- Epileptogenesis
- Epilepsy in children
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Treatments |
- Anticonvulsants
- Electroencephalography (diagnosis method)
- Epileptologist
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Personal issues |
- Epilepsy and driving
- Epilepsy and employment
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Seizure types
Epilepsy types |
Focal |
- Seizures
- Simple partial
- Complex partial
- Gelastic seizure
- Epilepsy
- Temporal lobe epilepsy
- Frontal lobe epilepsy
- Rolandic epilepsy
- Nocturnal epilepsy
- Panayiotopoulos syndrome
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Generalised |
- Tonic-clonic
- Absence seizure
- Atonic seizure
- Automatism
- Benign familial neonatal epilepsy
- Lennox-Gastaut
- Doose syndrome
- West
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Status epilepticus |
- Epilepsia partialis continua
- Complex partial status epilepticus
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Myoclonic epilepsy |
- Progressive myoclonus epilepsies
- Dentatorubral-pallidoluysian atrophy
- Unverricht-Lundborg disease
- MERRF syndrome
- Lafora disease
- Juvenile myoclonic epilepsy
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Non-epileptic
seizures |
- Febrile seizure
- Psychogenic non-epileptic seizures
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Related disorders |
- Sudden unexpected death in epilepsy
- Todd's paresis
- Landau-Kleffner syndrome
- Epilepsy in animals
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Epilepsy
organizations |
- Citizens United for Research in Epilepsy
- Epilepsy Action
- Epilepsy Action Australia
- Epilepsy Foundation (USA)
- Epilepsy Outlook (UK)
- Epilepsy Research UK
- Epilepsy Toronto
- International Dravet Epilepsy Action League
- Epilepsy Society
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Index of the central nervous system
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Description |
- Anatomy
- meninges
- spinal cord
- medulla
- pons
- fourth ventricle
- mesencephalon
- cerebellum
- diencephalon
- cortex
- association fibers
- commissural fibers
- lateral ventricles
- basal ganglia
- Physiology
- Development
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Disease |
- Meninges
- Demylinating diseases
- Seizures and epilepsy
- Headache
- Cerebrovascular
- Sleep
- Congenital
- Injury
- Neoplasms and cancer
- Other
- Symptoms and signs
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Treatment |
- Procedures
- Drugs
- general anesthetics
- analgesics
- addiction
- anticonvulsants
- cholinergics
- migraine
- parkinson
- vertigo
- other
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