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Pediatr Res. Author manuscript; available in PMC 2010 June 1.
Published in final edited form as:
PMCID: PMC2692092

The Role of Epilepsy and Epileptiform EEGs in Autism Spectrum Disorders


Autism is a neurodevelopmental disorder of unknown etiology characterized by social and communication deficits and the presence of restricted interests/repetitive behaviors. Higher rates of epilepsy have long been reported, but prevalence estimates vary from as little as 5% to as much as 46%. This variation is probably the result of sample characteristics that increase epilepsy risk such as sample ascertainment, lower IQ, the inclusion of patients with non-idiopathic autism, age, and gender. However, critical review of the literature reveals that the rate in idiopathic cases with normal IQ is still significantly above the population risk suggesting that autism itself is associated with an increased risk of epilepsy. Recently there has been interest in the occurrence of epileptiform electroencephalograms (EEGs) even in the absence of epilepsy. Rates as high as 60% have been reported and some investigators propose that these abnormalities may play a causal role in the autism phenotype. While this phenomenon is still not well understood and risk factors have yet to be determined, the treatment implications are increasingly important. We review the recent literature to elucidate possible risk factors for both epilepsy and epileptiform EEGs. We then review existing data and discuss controversies surrounding treatment of EEG abnormalities.

Autism and related autism spectrum disorders (ASD) are lifelong, often severely impairing neurodevelopmental syndromes involving deficits in social relatedness, language, and behavior. Reports of increasing prevalence, the lack of well controlled studies on treatment efficacy, and the immense costs of education and care for these patients all combine to make autism a public health crisis. However, despite a large body of careful pharmacological, pathological, electrophysiological, and imaging investigations, the etiology of autism remains unclear. Known medical conditions account for only a fraction (5-20%) of autism (1-3). Co-morbidity with other neurological disorders, demonstrated widespread neuropathological changes, and an emerging literature of structural and functional neuroimaging differences in autism all herald an underlying central nervous system (CNS) abnormality.

One of the best-known associations with CNS dysfunction is the high risk of epilepsy. This has been known since the first cases of autism (4) and is commonly reported to occur in 1/3 of individuals with ASD. However, the exact prevalence remains unknown and the literature presents a wide range of estimates from 5% (5) to 46% (6). ASD is also increased in epilepsy populations, with as high as 32% (7) meeting diagnostic criteria.

There is no primary seizure type or syndrome associated with autism. Complex partial (with or without secondarily generalized seizures), absence, and generalized tonic-clonic have all been reported (8-12). The diagnosis of seizure activity in autistic individuals is made more difficult because the behavioral abnormalities associated with complex partial and/or absence seizures (e.g., staring and non-responsiveness with or without repetitive motor behaviors) can all be attributed to the autism. Recently, there have also been reports of high rates of epileptiform EEGs in children with autism without a history of seizures or epilepsy (13, 14).

The increased prevalence of epilepsy and/or epileptiform EEG abnormalities in individuals with ASD may be an important clue to an underlying neurological abnormality, at least for a subset of autism patients. However, there are no definitive data to help predict which children will develop epilepsy and/or EEG abnormalities and to what degree cognition, behavior and other phenotypic characteristics are affected. Fundamental questions regarding the relationship among the occurrence of epilepsy, and the cognitive, language and behavioral deficits seen in autism are still unanswered: is this just an epiphenomenon of the underlying neural dysfunction in autism, or is there a causal relationship (15)?

A critical review of the literature points to several characteristics that appear to be associated with the presence of epilepsy in ASD including: IQ, additional neurogenetic disorders, age, developmental regression, and gender. This paper evaluates the association of these features with both clinical epilepsy and epileptiform EEG abnormalities in individuals with autism in an attempt to identify risk factors. We also review treatment strategies and discuss emerging ideas in this area.


Variability and Sample Characteristics

Table 1 provides rates from studies published since 2000 showing the wide range of estimates. Sample variability is most likely responsible for these disparities. Sample ascertainment strategies and inclusion of individuals with different cognitive levels, ages, and co-morbid medical conditions contribute to rate differences.

Table 1
Summary of studies published since 2000 examining the prevalence of epilepsy in ASD populations (total samples and special populations within sample such as those with and without intellectual disability (ID) or gender) including sample characteristics ...


Referral or ascertainment bias may be the most important confounding factor. Clinic based samples report higher rates, as patients with epilepsy are over-represented in these settings (6). Population based studies avoid this bias and provide the best estimate of true prevalence of epilepsy in autism, but even those rates have been variable. A review (16) of 9 population based studies reported epilepsy prevalence with a median of 17% and a range of 5-26%. Another long term follow-up study of a population based sample reported a substantially higher lifetime epilepsy prevalence of 38% (10). Clearly, other factors are at play in producing these variable rates.


It has been posited that the presence of intellectual disability drives the association between epilepsy and ASD. Certainly a high percentage of children on the autism spectrum have co-morbid intellectual disability (16) and intellectual disability is an independent risk factor for developing epilepsy (17).

Most studies have reported an association between low IQ and increased epilepsy in autism (8, 9, 11, 18-21). A meta-analysis of 10 studies demonstrated a higher pooled epilepsy prevalence rate in individuals with (21.5%) vs without, (8 %) intellectual disability (22). Also patients with both intellectual disability and active epilepsy have high rates of autism (8).

However, it should be noted that other studies show no statistically significant association between epilepsy and IQ in autism (23, 24), and the rate of epilepsy is still much above the general population risk even among individuals with normal IQ (22, 25). Thus, while intellectual disability increases the risk, it appears that autism itself is associated with higher epilepsy rates.


There is a small subset of ASD cases with known co-morbid medical conditions believed to be causally related; and these often have high rates of epilepsy themselves (Tuberous Sclerosis Complex, Fragile X syndrome, 15q duplication syndrome, among others) (2, 26, 27). These cases are referred to as non-idiopathic or syndromic, and their inclusion in autism samples inflates epilepsy prevalence estimates.

Studies have shown higher rates of epilepsy in non-idiopathic groups compared to idiopathic groups (2, 18) and studies limiting the sample to purely idiopathic autism reported lower rates of epilepsy (13 – 17% (11, 28)). Again, these rates in idiopathic ASD are still substantially above the general population risk of epilepsy (1-2%) suggesting that autism itself is associated with increased epilepsy risk.


There are two peaks in the age of onset of epilepsy in ASD (16, 19): first in early childhood and second (perhaps higher) in adolescence (11, 29). Thus, some of the variability in reported rates is simply a function of the age of the sample with some of the highest reported in studies including adolescents and young adults (6, 10, 30).


A noticeable loss of skills, or developmental regression, occurs in up to 1/3 of children with autism (31). The period of regression usually occurs between 18-24 months of age and can occur in those who were developing normally or in those with pre-existing developmental delays. Researchers have been interested in the phenomenon and its relationship to epilepsy because of the idea that an epileptic encephalopathy may play a role in the etiology of autism. However, results are inconsistent.

Several studies report statistically significant associations between the presence of regression and an increase in epilepsy (21, 32, 33). In contrast, other studies show no increases or associations between epilepsy and regression (11, 20, 28, 31). It is possible that other sample variables could be confounding factors; however, the relationship between regression and epilepsy in autism remains unclear.


Literature suggests an increased risk of epilepsy in females as opposed to males (6, 10, 24). A recent meta-analysis found the male to female ratio in autism with epilepsy was close to 2:1 vs. 3.5:1 in autism without epilepsy and a higher pooled prevalence of epilepsy in females than males (34.5% vs. 18.5%) (22). In contrast, another study of idiopathic autism reported no significant differences in gender ratios (11). It is unclear whether this is an effect of female gender per se or whether more females have other risk factors such as lower IQ and non-idiopathic autism.


As reviewed, there is an increased risk of epilepsy in ASD and many factors may further increase this risk. However, these factors may not exist independently in a given patient. For example, an individual may have a lower IQ because of a co-morbid neurogenetic syndrome that presents with early onset epilepsy. Unfortunately, existing studies have rarely had the sample sizes and phenotypic detail to determine which of these factors is most important in explaining the patient's increased epilepsy risk.

Future research that teases apart these features is imperative in order to accurately predict the individuals with ASD at increased risk of developing epilepsy. Furthermore, almost nothing is known about the relationship of epilepsy to the core features of autism: is the social domain more or less affected by epilepsy than language or repetitive behaviors? From a practical standpoint clinicians need to be aware of these risk factors in order to provide appropriate work-up and counseling to families. Neurogenetic disorders occur more frequently in the ASD patients with epilepsy and intellectual disability, often warranting specific diagnostic testing.


There are many reports of background or interictal EEG changes in individuals with autism. It is important to note that these abnormalities may occur in individuals without seizures, and their presence should not be considered evidence of epilepsy. Rather, these EEG changes are considered to be signs of cerebral dysfunction. Both nonspecific changes, such as slowing or asymmetry, and epileptiform discharges, consisting of spikes or sharp wave discharges, sharp slow waves, generalized spike-wave, and generalized polyspikes are seen. Epileptiform discharges are common among patients with active epilepsy, but are reportedly rare (1-4%) in healthy children (34, 35). One intriguing finding in ASD is the high rates of these abnormalities, even in the absence of epilepsy. This raises questions about whether these discharges could be considered a biomarker of cortical dysfunction in this population, and whether these discharges have a causal association with any of the autism phenotypes.

Much like rates of epilepsy, reported rates of epileptiform abnormalities are quite variable. This may be due to sample characteristics and/or the methodological variability in collecting and interpreting EEGs. Many studies report an overall EEG abnormality rate by combining individuals with and without epilepsy. Referral bias may also play a major role, as there are no population-based studies of rates of epileptiform discharges among individuals with ASD. Most reports are retrospective reviews of large clinic samples meaning that the clinical practice of the individual investigator will influence the data. Differences in EEG type (routine office studies vs. prolonged recording, whether sleep is captured) have also been shown to affect rates.

Rates Of Epileptiform Discharges

Until recently, reported rates of interictal epileptiform discharges varied from 6 to 30% of ASD patients (19, 20, 29, 31). Recently, even higher rates of isolated epileptifom EEGs have been reported (see Table 2).

Table 2
Summary of studies published since 2000 examining the prevalence of epileptiform EEGs in ASD populations (total samples and special populations within sample such as those without epilepsy).

Several studies have reported epileptiform abnormality rates of approximately 30% in ASD patients without clinical seizures (21, 36, 37). One study of children referred for video EEG monitoring to evaluate possible seizures found interictal epileptiform abnormalities in 59% (14). While some of the patients had a history of seizures, there were no seizures captured on monitoring so these were isolated epileptiform discharges. Interestingly, the history of epilepsy did not predict the likelihood of abnormalities in this cohort. A retrospective review of almost 900 children with ASD who had no known history of epilepsy, found 61% with epileptiform EEG activity in sleep (13). These latter studies are important because they show that this pattern could represent a common objective physiological finding in ASD, something that is difficult to find in this heterogeneous behaviorally defined condition.

However, lower rates (4-22%) were also reported in recent studies (11, 12, 28, 38). Some of these differences may be explained by methodological and sample differences. Some samples were purely idiopathic (11, 30). Others employed routine EEGs rather than prolonged studies which could lessen sensitivity (11, 12). Clearly, large prospective trials in unselected populations of autism are needed to determine the true rate of interictal epileptiform discharges. Data could help determine other risk factors and to delineate the role (if any) of these discharges in the autism phenotype.

Other variables affecting rates of isolated epileptiform discharges


As with epilepsy, the association with the occurrence of regression and epileptiform EEG abnormalities remains unclear. Currently many practitioners use the presence of regression as a rationale for obtaining an EEG, to rule out a specific type of epilepsy, Landau Kleffner Syndrome (see below). However, the literature contains incomplete and conflicting results that do not necessarily support this practice.

Studies which include only groups ascertained for regression have reported high rates of epileptiform EEGs, from 33-68% (39, 40). However, as a non-regression group was not included for comparison, it is not known whether there is something special about regression per se. Additionally, many studies do not separate the sample by those with and without epilepsy and so the influence of regression on epileptiform discharges in the non-epileptic sample cannot be determined.

In samples combining those with and without epilepsy, no significant association has been reported between regression and the presence of epileptiform EEGs (29, 31, 33). Similarly, even studies limited to children without epilepsy, report no significant effect of regression on epileptiform EEGs (13, 20). In contrast, at least two studies have found a two fold increase in epileptiform EEGs in those with regression (compared to without) (31, 37) in patients without epilepsy.


While it is known that lower IQ influences epilepsy rates, the effect of intellectual disability on the rate of isolated epileptiform EEGs is less well studied, and the existing data are conflicting. One study found no IQ differences between those with and without epileptiform EEGs (37), but another (31) reported that epileptiform EEG was significantly more common among individuals with intellectual impairment.


It appears that the rates of epileptiform discharges are influenced by the types of EEGs performed, with the highest rates in studies using overnight recordings (13, 14) or EEGs that include at least some sleep state recording (37). One study (13) reported the epileptiform activity was exhibited only in sleep states. Another study evaluated both types of EEG in the same patients and found that prolonged sleep EEG's significantly increased the yield of EEG abnormalities (21).

Patterns of EEG Abnormalities

If these abnormalities are taken as evidence of cortical dysfunction in autism, then examination of their types or patterns could shed light on the type of brain dysfunction. Epileptiform EEGs appear to be more common than non-epileptiform abnormalities (14, 21, 36, 38, 41). However, there appears to be no consistent pattern of epileptiform discharges across investigations with most studies reporting a variety. These include diffuse or generalized, multi-focal, and focal discharges, unilateral or bilateral and localized to many different brain areas (6, 11, 13, 28, 30, 38). Some studies suggest that temporal abnormalities may be more common (13, 37), but others do not support this view (14). The frequency of discharges is also variable (6, 33). Interestingly, it is rare to see the EEG pattern of electrical status epilepticus in sleep (ESES) associated with Landau Kleffner Syndrome (see below) in individuals with autism (12, 37).


The current literature would suggest that a substantial proportion of individuals with autism have epileptiform discharges in the absence of epilepsy. Yet, no clear picture emerges regarding risk factors. Nor do we have a consistent pattern of what these abnormalities might look like or what they mean. It is tempting to posit that these discharges are somehow causally related to the deficits (behavioral, communicative and cognitive) exhibited in ASD but there are very few data to support this idea.


The idea that epilepsy is somehow pathophysiologically related to ASD is supported by high epilepsy rates in related disorders. Epilepsy rates in Rett syndrome range from 63% to 94% (42, 43), and rates of up to 77% are seen in Childhood Disintegrative Disorder (CDD) (44). Rates in PDD-NOS are similar to those in autism (12) or perhaps somewhat lower (38). There is also a higher percentage of epilepsy and epileptiform EEGs in children with Developmental Language Disorder (DLD) (9, 45, 46). Likewise, there is some evidence of overlapping cognitive, language and behavioral deficits in autism spectrum disorders and other epilepsy syndromes supporting the possibility of a pathophysiological relationship.

Landau-Kleffner Syndrome

There has been much interest in the possible connection between autism and Landau-Kleffner syndrome (LKS). LKS is characterized by the rapid onset of an inability to understand spoken language in a typically developing child, usually accompanied by seizures (47). It is often associated with a severe EEG abnormality in deep sleep (electrical status epilepticus in sleep or ESES). LKS has been treated with traditional anticonvulsant medications, corticosteroids, intravenous immunoglobulins, and even epilepsy surgery (48). In many instances, both the seizures and language impairment improve with normalization of EEG abnormalities. However, the relationship between language deficits and seizures/EEG abnormalities is not completely clear. Seizures often occur only after the period of regression or not at all (15) and EEG findings do not always correlate with the severity and course of language impairment (49).

There is debate in the literature regarding whether the language regression and the accompanying EEG abnormalities in LKS can be likened to those seen in the subset of children with autistic regression and epilepsy (31, 48, 50). The term LKS or LKS variant is now used in clinical practice for individuals with autistic regression and epileptiform EEGs. Although caution is urged because of differences in the syndromes (48, 50), similar treatments are sometimes employed (see treatment section).

Tuberous Sclerosis

Tuberous Sclerosis Complex (TSC) is a rare neurogenetic condition characterized by abnormalities in multiple systems. CNS manifestations include structural brain lesions, frequent intellectual disability, and a high prevalence of epilepsy. While TSC is relatively uncommon (1-3%) in large unselected samples of individuals with ASD (51), it is more common among individuals with both autism and epilepsy (52). Autistic symptoms are frequent in children with TSC, and ASD has been reported in up to 60% of clinic samples (51, 53). The reason for development of ASD in TSC remains unknown, although early onset epilepsy and the presence of intellectual disability appear to be risk factors (52). It is hypothesized that electrophysiological dysfunction in the temporal lobe disrupts the development of social communication skills (54).

Infantile Spasms

Infantile spasms (IS) are a devastating early onset epilepsy syndrome with an associated severely abnormal background EEG pattern (hypsarrhythmia) and poor developmental outcome. Spasms appear to increase the risk of developing autism (55) and a percentage of ASD individuals have a history of spasms (23). In a recent study the presence of hypsarrhythmia and frontal lobe EEG discharges were both associated with the development of ASD in children with spasms (56). However, data suggest that it might be the cause underlying spasms rather than the spasms responsible for the increased ASD risk (57).

Benign Childhood Epilepsy Syndromes

Considered “benign” because of easy to control seizures and absence of cognitive or neurological impairment, Benign Epilepsy with Cento-Temporal Spikes (BECTS) (a.k.a Rolandic epilepsy) and Absence Epilepsy, are of interest because of emerging data suggesting subtle behavioral and cognitive problems in these patients. In BECTS these include: behavioral problems, learning disabilities, ADHD, mild cognitive and coordination deficits, and even specific language impairments (58). In Absence Epilepsy these include subtle cognitive and linguistic deficits and a high rate of psychiatric diagnoses (59). Thus, the presence of epilepsy and epileptiform EEGs appear to predispose individuals to cognitive, linguistic, and behavioral deficits.

Some of these associations between epilepsy syndromes (infantile spasms and LKS) and ASD raise a question about whether epilepsy and/or epileptiform EEGs may play any causal role in the development of autistic behaviors. One could posit that epilepsy could alter brain development with a resulting ASD phenotype. Alternatively, abnormalities in the underlying brain substrate might cause both the epilepsy and ASD. Unfortunately, there are presently no data to answer this question.



Treatment of children with autism and epilepsy is guided by the principles of treating childhood epilepsy. Anti-epileptic drugs (AEDs) are chosen based on seizure type and clinicians strive for maximum seizure control with minimum side effects. The practicalities of certain treatment choices are very important in ASD. Factors such as available formulations (liquid vs. tablets vs. capsules), dosing schedules, need for blood monitoring, and, most importantly, behavioral side effects must be considered. It is important to note that treating epilepsy does not usually have a major impact on the autism symptomatology. Some children may show improvements in cognition, communication, or behavior, but the autism diagnosis does not change.

EEG Discharges

Reports of high rates of interictal discharges are beginning to have an impact on clinical practices in autism. While EEGs are considered standard for all children with clinical or suspected seizures, whether an EEG should be performed in all children with autism is questionable, and whether to treat these discharges if they are discovered is controversial. The concept of “treating the EEG” is based on the hypothesis that discharges may have some causal relationship to the behavioral, language, or cognitive disturbance. In general, neurologists do not treat EEGs except in very specific cases (e.g., LKS, infantile spasms). Indeed, in clinical practice it is often considered “heretical” to contemplate this (see (54) author reply). However, this may be changing.

It has long been known that interictal discharges can interfere with normal neural processing (60, 61). Recently there has been more attention to the concept of deleterious transient cognitive impairment (TCI) due to the presence of background epileptiform discharges in patients with epilepsy (62, 63). Furthermore, there is an emerging focus on the frequent cognitive and behavioral disturbances in many childhood epilepsy syndromes (64). In BECTS, studies have shown that academic problems were related to the frequency of interictal epileptiform discharges (65) and attentional problems largely remitted after normalization of EEG (66). Thus, one could posit that treatment of EEG abnormalities would have a positive impact on symptomatology in children with ASD and epileptiform EEGs.

There are a few favorable case reports of EEG treatment in autism and other childhood epilepsy syndromes (60, 67, 68). Multiple case studies have demonstrated specific improvements in ASD symptoms after therapy to suppress discharges either with AEDs (69-71) or corticosteroids (72). It has even been suggested that the treatment of EEG discharges may prevent subsequent development of epilepsy (13). However, in the absence of results from controlled trials, the practice of medication use remains controversial.

Even more controversial is the use of epilepsy surgery (akin to those used in focal epilepsy and LKS). Several reports describe surgical treatment in individuals with autistic regression and intractable epilepsy. The degree of behavioral improvement was variable (73, 74) and not always related to clinical seizure control (75). Despite this, one study even extended the use of surgery to patients with epileptiform EEGs but without known seizures (40) and reported some of the patients had reduction of autistic features and improvements in language.

Unfortunately, all of these reports suffer the shortcomings of case studies, lacking controls and reliable or standardized outcome measures. Fortunately, several recent studies investigating the treatment of interictal EEG abnormalities with AEDs employ better methodology. One open label study using leviteracitam (an AED known to suppress interictal discharges) demonstrated remission of measurable auditory processing deficits in 4 of 6 children with BECTS (76). Both valproic acid and lamotrigine were shown in controlled trials to reduce interictal discharge burden and improve behavior in children with epilepsy (77, 78). However, it was noted that medication also reduced clinical seizure frequency, leaving open the possibility that better seizure control was responsible for the behavioral changes. A subsequent blinded placebo-controlled study of lamotrigine in children with well controlled epilepsy (79) spoke to this issue, finding behavioral improvement only in the children on active drug who had a significant reduction in either frequency or duration of their interictal discharges. This study suggests that the behavioral improvement from lamotrigine was the result of the discharge suppression, not seizure control or mood stabilization. However, not all results have been positive. A cross-over placebo- controlled trial using valproic acid in patients with epileptiform EEGs showed no improvement on any behavioral measure (80) and reported some cognitive and behavioral worsening in the drug phase, leading to a cessation of the trial.

At present, there are no controlled data investigating the efficacy of treating epileptiform EEG discharges in autism, but there is increasing interest in community practices. This void creates difficulties for both practitioners and families and makes controlled investigations of this phenomenon crucial. We propose that existing results are indeed intriguing and justify further exploration of the role of these discharges in the ASD population.


The search for genetic determination of this co-morbidity has stirred interest in a variety of genes implicated in both epilepsy and autism. For example GABA receptor genes are among the candidate autism susceptibility genes (81). Polymorphisms in sodium channel genes (82) and mutations in genes involved in synapse formation (neuroligins, neurexins, SHANK-3) (81) have been detected in some ASD families. Recently, converging evidence points to a role for CNTNAP2 (83-85)originally discovered in a family with epilepsy, cortical dysplasia and an autism like phenotype (86). Mutations in genes associated Rett Syndrome and its variants also predispose to epilepsy (87-91). Full discussion is beyond the scope of this review, but attention should be paid to this exciting new area that could help define pathophysiological mechanisms in both autism and epilepsy.


Despite the long recognized association between autism and epilepsy, surprisingly little is understood about the role epilepsy plays in ASD. Data from the literature suggest that lower IQ, age, gender and co-morbid medical conditions all increase epilepsy risk in the ASD population. However, in idiopathic autism samples without intellectual disability, epilepsy rates are still higher than the general population risk, suggesting that the underlying pathophysiology in ASD also increases the risk of epilepsy. Even less well studied, is the high rate of epileptiform EEGs in ASD without epilepsy. This is important to highlight because of treatment implications. If there is some causal relationship between the discharges and the ASD phenotype, and a substantial percentage of patients have epileptiform abnormalities, then there are a large number of individuals with ASD who could conceivably benefit from treatment. On the other hand, epileptiform abnormalities could be simply an epiphenomenon of the neuropathological process responsible for autism and have no relevance to prognosis or intervention.

Most recent reviews of this topic conclude with a statement about the lack of “convincing evidence” in the literature regarding the exact nature of the association between autism and epilepsy, especially regarding treatment options (48, 50). We believe that it is past time that we get some and would propose the following key elements in creating a research agenda.

  • Large population based studies to determine the true risk of epilepsy in individuals with ASD – including detailed medical, genetic and behavioral phenotyping to allow for determination of risk factors and prognosis.
  • Studies of large cohorts of unselected samples with prolonged EEGs and detailed phenotypic data to determine the frequency and character of abnormalities and investigate associations between types of epilepsy and EEG abnormalities and elements of the ASD phenotype (does the autism look the same?).
  • Controlled intervention trials to determine if the treatment of epileptiform EEGs has clinical utility. Positive results would offer a completely new treatment option for a large percentage of individuals with autism. However, negative data would allow clinicians to avoid subjecting patients to a needless (sometimes onerous) medical procedure and prevent exposure to unnecessary and potentially toxic medications or dangerous surgical interventions.

The ultimate question is one of causality: Is there a causal relationship between the EEG discharges and the ASD phenotype, and, if so, what does it mean for prognosis and intervention? Or, are the epileptiform discharges simply an epiphenomenon of the neuropathological process responsible for autism? Answers to some of these questions are crucial for formulation of much needed appropriate practice parameters both for work-up and treatment of individuals with ASD.


Financial Support: This work was supported by the intramural research program of the NIMH, XFF 80100.


Anti-epileptic Drug
Autism Spectrum Disorder
Benign Epilepsy with Centrotemporal Spikes
Central Nervous System
Intelligence Quotient
Landau Kleffner Syndrome
Tuberous Sclerosis Complex


This work was written as part of the authors' official duties as Government employees. The article is freely available for publication without a copyright notice, and there are no restrictions on its use, now or subsequently. The views expressed in this chapter do not necessarily represent the views of the NIMH, NIH, HHS, or the United States Government.


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