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Pediatric Neurology

At What Age Does Rolandic Epilepsy Usually Go Away?

At a Glance

Rolandic epilepsy, also called SeLECTS, usually resolves by puberty or the mid-teen years. Most children stop having clinical seizures by age 15 or 16, although some may continue until about 18; doctors judge remission mainly by a sustained seizure-free period, not one EEG.

Rolandic epilepsy, also known as Self-limited epilepsy with centrotemporal spikes (SeLECTS), usually goes away on its own by puberty or the mid-teen years [1][2]. While the exact timing varies, most children stop having seizures by age 15 or 16, though for some it may take up to approximately age 18. Doctors primarily base the medical “all clear”—meaning the epilepsy has likely resolved—on a prolonged period free from any clinical seizures, rather than relying strictly on tests [3].

The Timeline to Remission

The term “self-limited” means that the condition is expected to resolve naturally as your child’s brain matures [1]. While remission is the most common outcome, there is no single guaranteed date when this will happen.

The timeline can sometimes be influenced by when the condition first began. For example, children diagnosed very early—particularly before age 5—may take somewhat longer to achieve complete seizure control [4][5]. However, the treating neurologist will interpret your child’s age of onset together with their seizure type, development, and response to treatment. If seizures change, become frequent during the day, or if you notice developmental regression, contact your neurologist, as this may require a prompt reassessment of the diagnosis.

How Doctors Confirm Remission

Parents understandably want a specific test to confirm their child is “cured.” However, doctors evaluate remission through an individualized clinical assessment, not a single test:

  • A Prolonged Seizure-Free Period: The most critical sign of remission is that your child stops having clinical seizures [3]. This means no nighttime events, but also no subtle daytime symptoms. Seizures in SeLECTS can include speech arrest (inability to speak), throat or swallowing sounds, drooling, unusual sensory symptoms, one-sided facial or limb jerking, or a generalized convulsion. Your pediatric neurologist will watch for a sustained period without any of these events [3].
  • The Role of the EEG: An EEG (electroencephalogram) measures electrical patterns in the brain. In SeLECTS, doctors look for centrotemporal spikes—which are characteristic EEG wave patterns, not seizures themselves [6]. While your doctor might order a follow-up EEG, a “clean” EEG is not universally required to declare remission. Centrotemporal spikes can sometimes persist even after clinical seizures have permanently stopped, and an abnormal EEG does not necessarily mean the epilepsy is still actively causing physical symptoms [6][7]. Conversely, a normal EEG does not guarantee that seizures will never return [6]. The EEG is just one piece of the puzzle used to inform follow-up care.

Medication Withdrawal

If your child is taking antiseizure medication, never stop or reduce the dose on your own, even if they have been seizure-free or had a normal EEG. Tapering medication is a highly individualized process [8][9]. A normal EEG is not the deciding criterion for weaning; instead, your doctor will discuss a gradual tapering plan based on clinical history, age, and syndrome features.

Monitoring Beyond the Seizures

Even after the physical seizures have stopped, follow-up appointments remain important. SeLECTS can sometimes be associated with difficulties in language, learning, attention, or thinking skills [10][11].

While these cognitive and attention issues can improve for some children once the condition goes into remission [12], improvement is not guaranteed. Do not wait for remission if you notice learning struggles. Discuss these concerns with your care team, who can help arrange school accommodations or formal neuropsychological testing (specialized testing to evaluate memory, learning, and attention) independently of whether the EEG has normalized [10][12].

When to Seek Urgent Help

Even if your child has been seizure-free for a long time, it is vital to know when to seek emergency medical care. Follow your child’s seizure action plan and call for urgent help if:

  • A seizure lasts 5 minutes or longer
  • Repeated seizures occur without full recovery in between
  • Your child has difficulty breathing or is seriously injured
  • They experience a first or new type of seizure

Common questions in this guide

When do most children with Rolandic epilepsy become seizure-free?
Most children with Rolandic epilepsy stop having clinical seizures by age 15 or 16, often around puberty or the mid-teen years. Some children may continue to have seizures until approximately age 18. The exact timing depends on the child’s seizure history and other clinical features.
How does a neurologist decide that Rolandic epilepsy is in remission?
Doctors usually consider remission when a child has had a prolonged period without any clinical seizures, including subtle nighttime or daytime events. A follow-up EEG may help guide care, but a normal EEG is not always required.
Can EEG abnormalities remain after Rolandic epilepsy seizures stop?
Yes. Centrotemporal spikes can remain on an EEG after clinical seizures have stopped, while a normal EEG does not guarantee that seizures will never return. The EEG is one part of the neurologist’s overall assessment.
How is seizure medicine safely stopped after remission?
Do not stop or reduce antiseizure medicine without speaking with your child’s neurologist. If withdrawal is appropriate, the neurologist will use a gradual, individualized taper based on the seizure history, age, and features of the epilepsy.
Could learning or attention problems continue after the seizures end?
Some children with SeLECTS have difficulties with language, learning, attention, or thinking even after seizures stop. These concerns may improve but are not guaranteed to do so, so ask the care team about school support or specialized testing of memory, learning, and attention regardless of the EEG result.
What seizure changes require emergency medical help?
Seek emergency help if a seizure lasts 5 minutes or longer, seizures repeat without full recovery, your child has trouble breathing or a serious injury, or your child has a first or new type of seizure. Follow the child’s seizure action plan while waiting for help.

Questions to Ask Your Doctor

Curated prompts to bring to your next appointment.

  1. 1.Why are you recommending (or not recommending) a follow-up EEG at this stage, and how will its result change our management plan?
  2. 2.Now that my child has been seizure-free, what is the safest timeline and gradual process for discussing medication weaning?
  3. 3.What specific subtle events, like speech arrest or drooling, should I watch for that might indicate a clinical seizure?
  4. 4.Should we consider formal neuropsychological testing or school accommodations to evaluate my child's language and learning skills right now?
  5. 5.If we eventually taper off the medication and a seizure occurs, what exactly is our immediate action plan?

Questions For You

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References

References (12)
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    Beta oscillations in the sensorimotor cortex correlate with disease and remission in benign epilepsy with centrotemporal spikes.

    Song DY, Stoyell SM, Ross EE, et al.

    Brain and behavior 2019; (9(3)):e01237 doi:10.1002/brb3.1237.

    PMID: 30790472
  2. 2

    Self-limited epilepsy with centro-temporal spikes: A study of 46 patients with unusual clinical manifestations.

    Galicchio S, Espeche A, Cersosimo R, et al.

    Epilepsy research 2021; (169()):106507 doi:10.1016/j.eplepsyres.2020.106507.

    PMID: 33296810
  3. 3

    Epileptic Negative Myoclonus as the First and Only Symptom in a Challenging Diagnosis of Benign Epilepsy With Centrotemporal Spikes.

    Chen J, Zheng G, Guo H, et al.

    Child neurology open 2017; (4()):2329048X17715965 doi:10.1177/2329048X17715965.

    PMID: 28815192
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    Self-Limited Epilepsy with Centrotemporal Spikes in Younger Ages: Worse but Real!

    Donbaloğlu F, Yanartaş MS, Tsakir C, et al.

    Annals of Indian Academy of Neurology 2025; (28(5)):699-704 doi:10.4103/aian.aian_466_25.

    PMID: 41082184
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    [The atypical developments of rolandic epilepsy are predictable complications].

    Pesántez-Ríos G, Martínez-Bermejo A, Arcas J, et al.

    Revista de neurologia 2015; (61(3)):106-13.

    PMID: 26178515
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    Serial changes in the paroxysmal discharges in rolandic epilepsy may predict seizure recurrence: A retrospective 3-year follow-up study.

    Arhan E, Serdaroglu A, Ozturk Z, et al.

    Epilepsy & behavior : E&B 2018; (82()):150-154 doi:10.1016/j.yebeh.2018.03.014.

    PMID: 29625366
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    The Prevalence and Risk Factors of Electrical Status Epilepticus During Slow-Wave Sleep in Self-Limited Epilepsy With Centrotemporal Spikes.

    Lu G, Cheng Y, Wang Y, et al.

    Clinical EEG and neuroscience 2024; (55(2)):265-271 doi:10.1177/15500594231182758.

    PMID: 37331959
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    The fate of spikes in self-limited epilepsy with centrotemporal spikes: Are clinical and baseline EEG features effective?

    Günay Ç, Sarikaya Uzan G, Özsoy Ö, et al.

    Epilepsy research 2023; (193()):107165 doi:10.1016/j.eplepsyres.2023.107165.

    PMID: 37201400
  9. 9

    The Efficacy and Cognitive Impact of Perampanel Monotherapy in Patients with Self-Limited Epilepsy with Centrotemporal Spikes: A Retrospective Analysis.

    Yue X, Liu XM, Chen J, et al.

    Neuropsychiatric disease and treatment 2023; (19()):1263-1271 doi:10.2147/NDT.S410858.

    PMID: 37274142
  10. 10

    Neurocognitive effects and electrophysiological findings in ADHD and self-limiting centrotemporal spike wave epilepsy (SeLECTS) - A prospective tertiary care study.

    Orak SA, Bilaç Ö, Polat M, et al.

    Epilepsy & behavior : E&B 2024; (157()):109900 doi:10.1016/j.yebeh.2024.109900.

    PMID: 38909461
  11. 11

    The attention networks in benign epilepsy with centrotemporal spikes: A long-term follow-up study.

    Wu L, Yang X, Wang X, et al.

    Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2021; (88()):22-27 doi:10.1016/j.jocn.2021.03.022.

    PMID: 33992188
  12. 12

    Children with Rolandic epilepsy have micro- and macrostructural abnormalities in white matter constituting networks necessary for language function.

    Ostrowski LM, Chinappen DM, Stoyell SM, et al.

    Epilepsy & behavior : E&B 2023; (144()):109254 doi:10.1016/j.yebeh.2023.109254.

    PMID: 37209552

This page explains when Rolandic epilepsy may remit and how doctors assess it for informational purposes only; it does not constitute medical advice. Do not change your child’s antiseizure medication without guidance from the child’s neurologist.

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