Overview of Atonic Seizures

This condition is most common in children

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Atonic seizures (also known as drop attacks) are one of several types of seizures that can occur as a result of various underlying causes. “Atonic” means loss of muscle tone. This type of seizure is also known as akinetic or drop seizures.

Atonic seizures oftentimes begin during childhood and are most common in children, although they may continue into adulthood. This type of seizure is often present in people who have other types of seizures as well, such as tonic or myoclonic seizures.

Atonic seizures are rare, accounting for less than 1% of all seizures.

Woman with daughter at doctor's office
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Overview of Seizures

Neurons, or nerve cells in the brain, communicate with each other constantly by transmitting electrical impulses from one to another. Voluntary and involuntary movement is controlled and regulated by these nerve transmissions.

A seizure is the result of the brain receiving surges of abnormal electrical signals, interrupting normal electrical brain functioning in the nerve cells that control the muscles. Primarily, there are two types of seizures: generalized and focal. The difference is mainly where they begin in the brain.

Generalized seizures involve the entire brain, and subsequently, affect the entire body. They may also cause convulsions (non-voluntary movements), but some generalized seizures (such as absence seizures) do not cause convulsions. There are six types of generalized seizures:

  • Absence (petit mal)
  • Atonic
  • Tonic-clonic (grand mal)
  • Clonic
  • Tonic
  • Myoclonic

Focal seizures (also called partial seizures) are those that start in one part of the brain and affect the part of the body controlled by that part of the brain. Depending on the type of seizure, an atonic seizure can also be focal.

What Are Atonic Seizures?

Normally, when you sit or stand, your muscles are slightly contracted. That allows the body to stay upright. 

In an atonic seizure, a person’s muscles do not clench up as they do in the more well-known types of seizures called tonic-clonic (convulsive or grand mal) type. 

In fact, the muscles become so relaxed that the person having atonic seizures often falls forward because the muscles are unable to support the body. If they're standing, they'll fall to the ground.

If the person is sitting, an atonic seizure may make their head drop. This is typical of babies who are too young to stand, as well. It can be difficult to spot an atonic seizure in a person who's lying down except that they become limp and unresponsive. 

Atonic seizures are less common than many other types of seizures, but they can occur in conjunction with other types. 

An atonic seizure may begin with one or more myoclonic jerks. This type of seizure is usually short in duration, coming on without warning. Recovery is usually quick, as well (excluding any injuries that may occur from falling). Falls from atonic seizures often result in injuries to the face and head.

Atonic seizures cause a person’s muscles to suddenly become flaccid. 

Types of Atonic Seizures

Atonic seizures can be categorized as focal seizures (starting in one part of the brain) and cause muscle tone loss in only one part of the body. This is referred to as a focal motor atonic seizure.

When the atonic seizure starts on both sides of the brain, it is referred to as a generalized onset atonic seizure.  Most of the time, atonic seizures are generalized seizures. Generalized atonic seizures start out with a sudden loss of muscle tone in the head, the trunk, or the entire body. 

Atonic seizures usually result in loss of consciousness. This type of seizure normally lasts less than 15 seconds but may last up to several minutes. After an atonic seizure, a person will quickly become alert and conscious.


Symptoms of atonic seizures may include:

  • A sudden loss of muscle strength
  • Going limp and falling to the ground
  • If seated, the person’s head will appear to suddenly drop down
  • Remaining conscious or experiencing a brief loss of consciousness
  • Drooping eyelids
  • Head nods
  • Jerking movement


Anything that disrupts the normal nerve transmission in the brain can cause a seizure. This can include:

  • A very high fever
  • Low blood sugar
  • High blood sugar
  • Alcohol or drug withdrawal
  • A brain concussion (from an injury to the head)
  • Strokes
  • Some types of illnesses
  • A brain tumor
  • Other factors

Common causes of seizures in infants include:

  • Imbalance of neurotransmitters (chemical messengers in the brain)
  • Genetics
  • Brain tumor
  • Stroke
  • Brain damage, usually due to illness or injury
  • Low blood sugar levels
  • Mother's use of certain drugs during pregnancy
  • Birth trauma, including lack of oxygen (hypoxic-ischemic encephalopathy)
  • Low calcium or magnesium in the blood
  • Infections such as meningitis or encephalitis
  • Brain hemorrhage (bleeding), which may be due to being born very early
  • High fevers (not usually associated with epilepsy)
  • Other unknown factors

Risk Factors and Triggers

The underlying cause of atonic seizures is often unknown. Changes in the genes may be responsible for an increased risk of having atonic seizures. In fact, researchers have identified nearly a thousand genes that play a role in epilepsy. 

Children are most often affected by atonic seizures, but this type of seizure can occur at any age. Triggers for atonic seizures may include hyperventilation (fast breathing) and/or flickering lights.

Atonic Seizures in Epilepsy

When a person has two or more seizures of any type, they are diagnosed with epilepsy of unknown cause.

Epilepsy affects about 3.4 million people in the United States, according to the Centers for Disease Control and Prevention. It’s one of the most common nervous system disorders. 

Atonic seizures are commonly the type of seizure experienced with specific types of epilepsy, such as Lennox-Gastaut syndrome (LGS) and Dravet syndrome (DS).

LGS is a severe childhood form of epilepsy involving:

  • Medication refractory seizures (when medication doesn't reduce the seizure episodes)
  • Drop attacks (atonic seizures)
  • Atypical absence seizures

Atypical absence seizures involve a less abrupt onset type of seizure compared to typical absence seizures, associated with loss of muscle tone in the trunk, limbs, or head and a gradual slump as well as mild myoclonic jerks.

Dravet syndrome (DS) is a severe form of epilepsy that includes symptoms such as:

  • Frequent, prolonged seizures often triggered by high body temperature (hyperthermia)
  • Developmental delay in infants and children
  • Speech impairment
  • Ataxia (loss of full control of body movements)
  • Hypotonia (an abnormally low level of muscle tone)
  • Sleep disturbances
  • Orthopedic conditions
  • Chronic infections
  • Dysautonomia (disruptions in homeostasis)
  • Other health problems

When to See a Healthcare Provider

The first time anyone has a seizure (of any type) the healthcare provider should be notified immediately and diagnostic steps should be made, including an examination of the medical history and a physical exam. 

In someone diagnosed with epilepsy, it’s important to seek immediate medical attention in any of the following scenarios:

  • A seizure lasting longer than five minutes
  • Breathing that doesn’t normalize after the seizure is over
  • Unconsciousness that lingers after the seizure is over
  • A second seizure that occurs after the first (cluster seizure)
  • A high fever occurs
  • Heat exhaustion is experienced
  • A seizure occurs during pregnancy
  • Any time diabetes is diagnosed
  • When an injury occurs due to a seizure


Whenever a person has a seizure, it’s imperative that the healthcare provider discern the type of seizure and which area of the brain is involved. This is because the anti-seizure medication regimen is partially based on the type and duration of seizures.

Input from observers (via written descriptions or video recordings) describing the event is an important part of the diagnostic assessment.

An electroencephalogram (EEG) is the primary diagnostic tool used to diagnose seizures. The EEG procedure involves attaching electrodes to the scalp to measure the electrical activity in the brain and reveal abnormal patterns. 

Various types of seizures can be identified by observing these patternsEEG tests are also conducted to measure the effectiveness of anti-seizure medications by testing how the drugs help with the electrical malfunction in the brain.

Magnetic resonance imaging (MRI) and computed tomography (CT) scans are also used to study important factors such as where the seizure occurs in the brain. These scans are often used to rule out possible causes of seizures such as a stroke.

If a diagnosis isn’t clear and anti-seizure medication isn’t effective, tests may be done to find other origins of the problem that could be causing the falls.


The goal in treating atonic seizures is to control, decrease the frequency of, or stop the seizures without interfering with a person’s normal life activities. The treatment for atonic seizures depends on many factors, including:

  • Properly identifying the type of seizures
  • Assessing the frequency of seizures
  • Diagnosing the underlying cause of the seizures (when possible)
  • The person’s age, health status, and medical history
  • Evaluation of the person’s medication tolerance and/or tolerance of other types of treatment

Factors that impact treatment options include:

  • The treatment goals
  • Preferences of the parents or person with seizures (in adult patients)
  • Side effects
  • The cost of the medicine
  • Adherence with the use of the medicine

In addition to medication, the healthcare provider will most likely encourage:

  • Proper rest to avoid sleep deprivation (which may trigger seizures)
  • Avoiding other things that trigger a seizure (such as flashing lights, a fever, and heat exhaustion)
  • Wearing a helmet to protect the head from fall-related injuries

Anti-Seizure Medication Administration

The healthcare provider will take several factors into consideration when prescribing anti-seizure medications. These include:

  • Using the type of anti-seizure medication that is specific for the type of seizure
  • Prescribing the lowest dose that will achieve seizure control
  • Administering frequent blood and urine tests to ensure proper medication management

Types of Medication

Anti-epileptic or anti-seizure drugs are the most common form of treatment for seizures; however, it may take the healthcare provider some time to discover the right drug and the best dosage for each person. 

Types of anti-seizure medication include:

  • Ethosuximide (Zarontin), which is commonly used as the first choice in anti-seizure drug treatment
  • Valproic acid, which is not recommended for women who are pregnant or of childbearing age because this medication can cause an increased risk of birth defects
  • Lamotrigine (Lamictal), which may be less effective than ethosuximide or valproic acid but has fewer side effects
  • Clobazam (Onfi)
  • Fenfluramine (Fintepla)

Taking Anti-Seizure Medicine

Always take anti-seizure medication exactly as prescribed by the healthcare provider (including scheduled time and dosage). Discuss possible side effects and report any that occur to the healthcare provider as soon as possible.

Anticipate that several tests will be performed to measure the effectiveness and safety of anti-seizure medications. These tests may include:

  • Frequent blood work and urine tests to measure the optimal level (called the therapeutic dose) that works best to control seizures with minimal side effects
  • Other types of tests to measure the effectiveness of anti-seizure medications in the body, such as EEGs

Consult with your healthcare provider about any activity restrictions due to side effects (such as drowsiness) caused by anti-seizure medications. Many people taking these drugs are encouraged to avoid operating heavy machinery.

Ask your healthcare provider or pharmacist before taking other medications (including over the counter drugs) because they may interfere with the effectiveness of anti-seizure medications or cause harmful side effects.

Drugs don't work for everyone, so your healthcare provider may recommend other kinds of treatment.

The Ketogenic Diet

Ketogenic diets are shown by research to help control seizures for some patients who don’t respond to medications. This low-carbohydrate, high-fat diet is most often used to treat children with epilepsy.

The ketogenic diet tricks the body into a state of starvation from the lack of carbohydrates and results in a state of ketosis in the brain. It was identified nearly a century ago, and in the past 30 years, studies have backed up its ability to lessen seizures in kids who don't respond well to anti-seizure medication.

"The connection between metabolism and epilepsy has been such a puzzle," said Gary Yellen, Ph.D., professor of neurobiology at Harvard Medical School. He was introduced to the ketogenic diet through his wife, Elizabeth Thiele, MD, Ph.D., HMS professor of neurology, who directs the Pediatric Epilepsy Program at Mass General Hospital for Children.

"I've met a lot of kids whose lives are completely changed by this diet, it's amazingly effective, and it works for many kids for whom drugs don’t work," said Yellen.

Surgical Procedures

Surgical options may be right for some people who don't respond well to medications.

Vagus Nerve Stimulator (VNS): VNS is a surgically implanted device that is sometimes implanted (and used in conjunction with anti-seizure medications) to help prevent seizures by sending small electrical impulses through a nerve in the neck—called the vagus nerve—to the brain.

A study published in 2013 discovered that while VNS was effective in lowering the incidence of some types of seizures (tonic-clonic and myoclonic type), it was ineffective at reducing atonic or tonic seizures in children with Lennox-Gastaut or Lennox-like syndrome.

Corpus Callosotomy: A surgical procedure called a corpus callosotomy (CC) is an operation aimed at interrupting the abnormal electrical activity in the brain, which spreads from one hemisphere to the other during a generalized seizure (such as an atonic seizure).

This is done by severing (cutting) the corpus callosum—an area of the brain located between the two hemispheres. This does not usually stop the seizures; they continue on the side of the brain in which the seizures start. 

Surgery is not recommended for everyone with atonic seizures, but it may be a good option for some. A 2015 study involving patients with atonic seizures and drop attacks undergoing CC and VNS discovered that 58% of those who had CC performed were free of atonic seizures after the procedure, compared to only 21.1% of the study subjects who had VNS implants.


The prognosis or projected outcome of atonic seizures depends primarily on the cause. Sometimes epilepsy syndromes (epilepsy of unknown cause) will go away once a child grows older. 

Usually, a child must be seizure-free for one or two years before the option to stop anti-seizure medication is considered. Adults typically have to be seizure-free for longer before healthcare providers recommend stopping medication. According to a 2019 study, the recommendation is at least two years.

In other instances, a child with atonic seizures may end up needing to take anti-epileptic medications for the rest of their life. Be sure you're making this decision with guidance from your healthcare provider so you're not taking undue risks with your health.

15 Sources
Verywell Health uses only high-quality sources, including peer-reviewed studies, to support the facts within our articles. Read our editorial process to learn more about how we fact-check and keep our content accurate, reliable, and trustworthy.
  1. American Epilepsy Society. Facts and Figures.

  2. Epilepsy Foundation. Atonic Seizures.

  3. Cedars-Sinai. Atonic Seizures.

  4. Stanford Children's Health, Lucile Packard Children's Hospital. Epilepsy and Seizures in Children.

  5. Merck Manual. Seizures in Children.

  6. Epilepsy Action/British Epilepsy Association. Epilepsy in babies.

  7. Wang J, Lin ZJ, Liu L, et al. Epilepsy-associated genes. Seizure. 2017;44:11-20. doi:10.1016/j.seizure.2016.11.030

  8. Centers for Disease Control and Prevention. Epilepsy Data and Statistics.

  9. Dravet Syndrome Foundation. What is Dravet Syndrome?

  10. D'Andrea Meira I, Romao TT, Pires do Prado JH, et al. Ketogenic diet and epilepsy: What we know so far. Front Neurosci. 2019;13:5. doi:10.3389/fnins.2019.00005

  11. Poorshiri B, Barzegar M, Tahmasebi S, et al. The efficacy comparison of classic ketogenic diet and modified Atkins diet in children with refractory epilepsy: a clinical trial. Acta Neurol Belg. 2019. doi:10.1007/s13760-019-01225-0

  12. Cukiert A, Cukiert CM, Burattini JA, et al. A prospective long-term study on the outcome after vagus nerve stimulation at maximally tolerated current intensity in a cohort of children with refractory secondary generalized epilepsy. Neuromodulation. 2013;16(6):551-6. doi:10.1111/j.1525-1403.2012.00522.x

  13. Rolston JD, Englot DJ, Wang DD, Garcia PA, Chang EF. Corpus callosotomy versus fabus nerve stimulation for atonic seizures and drop attacks: A systematic review. Epilepsy Behav. 2015;51:13-7. doi:10.1016/j.yebeh.2015.06.001

  14. Hixson JD. Stopping antiepileptic drugs: when and why? Curr Treat Options Neurol. 2010;12(5):434-42. doi:10.1007/s11940-010-0083-8

  15. Lossius MI, Alfstad KA, Aaberg KM, Nakken KO. Discontinuation of antiepileptic drugs in seizure-free patients - when and how? Tidsskr Nor Laegeforen. 2017;137(6):451-454. doi:10.4045/tidsskr.16.0957

Additional Reading

By Sherry Christiansen
Sherry Christiansen is a medical writer with a healthcare background. She has worked in the hospital setting and collaborated on Alzheimer's research.