We admitted to our department, a 13-year-old right-handed female patient, with a medical history of a neonatal right frontal stroke. She had no other significant personal or family history. She didn't undergo any genetic exploration, to our knowledge. Neurological examination showed a mild left hemiparesis, limited to a difficulty to precise movements in the left hand and a spasticity of the left lower limb. The patient had no cognitive deficits. She was attending school at the normal grade for her age. She was followed by pediatricians and rehabilitation specialists for her neonatal handicap.

Her first epileptic seizure was bilateral tonic-clonic and occurred at six years old. A 15 days post-seizure electroencephalogram (EEG) was normal and no treatment was started. Follow-up EEGs showed right frontal spikes. Subsequently, the patient had two similar seizures (at 1 year interval). Since these seizures were rare, the neuro-pediatricians did not retain the diagnosis of epilepsy and therefore did not start an anti-seizure medication. Three years later, a new type of seizures appeared. These began with paresthesia in the left arm, which sometimes expanded to the left lower limb. As a consequence, the left upper limb would reach a tonic position (flexion of the elbow and the wrist) with an inconstant involvement of the lower limb. At this stage, seizures either stopped, or resulted in a loss of consciousness and a secondary tonic-clonic generalization. Surprise, fear, and surprising "metallic" noises were the main triggering factors. The patient also reported nocturnal seizures, associated with nightmares. The frequency of these seizures increased rapidly, up to twelve episodes per day, with secondary generalization every 3 to 4 days. She was treated with Levetiracetam (500 mg twice a day, according to weight) during 6 months. Because of the absence of improvement, she was switched to Oxcarbazepine in March 2020 and had a decrease in the frequency of seizures. EEG inconstantly showed right frontal spikes. In brain MRI she had a porencephalic cavity in the right frontal lobe. The patient was referred to a neurologist for advice on this "paroxysmal dystonia". During the consultation, a seizure was provoked when the patient was surprised by the fall of a bunch of keys on the ground suggesting an underlying epileptic origin. The patient was referred to our epileptology tertiary “center for rare epilepsy” for an etiological assessment.

We performed sleep and wake video EEG recordings during five days with hyperventilation, intermittent light stimulation, and surprise stimulation to trigger seizures. We also reduced by half the dosages of Oxcarbazepine and maintained the patient awake during the first night of hospitalization. The patient did not receive benzodiazepine during these recordings.

Interictal EEG recordings showed abundant spike activity over the right frontal and central electrodes (Figure 1). We also recorded less frequently, more posterior spikes (over right centro-parietal electrodes). In slow-wave sleep, we found short bilateral fast activity discharges, with an initial right frontal component, not associated with a clinical event (Figure 2).

We could record ten seizures during the hospitalization. These seizures occurred mainly during the day, immediately after a surprising stimulus caused a startle reaction; meanwhile one seizure occurred spontaneously during the night. These ten seizures had similar clinical and EEG characteristics (Figure 3).

Clinically, after hearing a surprising noise, the patient had a startle reaction, followed by a tonic grimace of the face. Immediately thereafter, the left upper limb was in a tonic flexion (flexion of the forearm and the hand). During some seizures, a tonic contraction of the lower limb also occurred (flexion of the thigh and the hallux). The tonic posture lasted about 10 seconds and then resolved. There was no loss of consciousness. The patient reported that paresthesia in the left upper limb preceded the motor symptoms. We did not record seizures with secondary tonic-clonic generalization. During the immediate post-critical examination, the patient had a major motor deficit of the left upper limb.

Interpreting ictal EEG was difficult because of the initial startle artifact (Figure 3). The seizure probably started as a sharp wave over electrode Cz was recorded. Then, there was a discharge of fast activity on right and median fronto-central electrodes (Fp2, F4, Fz, Cz). We performed several provocative tests to determine which sensory modalities were involved in the triggering of seizures. Tactile stimulation, whether or not startling, of the left upper limb did not cause a seizure. Surprising visual stimulation (throwing objects) did not trigger seizures. Seizures were only triggered by surprising noises (e.g., loud call). Noises did not trigger seizures if the patient was informed previously.

We hypothesize that the generator of the seizures was in the right sensory-motor cortex. We pursued treatment with Oxcarbazepine (600 mg, twice a day) and combined it with Clobazam (5 mg, twice a day) for long-term treatment. At follow-up, the patient and her family reported a decrease in the frequency of focal seizures to once to twice a day and the absence of generalized seizures. The treatment was well tolerated, except for a slight drowsiness. The neuropsychological assessment revealed a delay in execution and a slight deficit in working memory.

Considering the usual pharmaco-resistance of this type of epilepsy, we offered our patient to start a presurgical evaluation. Because of the pandemic, the patient could not benefit from an intracranial recording by SEEG. We are also awaiting a functional motor MRI.

This case highlights that the clinical and electrophysiological diagnosis of startle epilepsy is not always easy. The diagnosis should be considered in paroxysmal dystonic movements with a stereotyped triggering factor, even if other non-suggestive seizures of reflex epilepsy have occurred previously.

This case also illustrates the importance of repeating the EEG recordings for a precise analysis considering artifacts and pseudo normal patterns during the seizure. In this patient's case, we suggest surgery. A pre-surgical assessment must be very rigorous in the case of patients with mild motor and cognitive deficits, so as to avoid major postoperative complications. The limitations of our case are the lack of follow-up data, as the patient could not benefit from intracranial recordings, and the difficulties of interpreting the ictal EEG.

Startle epilepsy was first described in 1955 by Alajouanine and Gastaut [1]. Since then, the literature has been enriched by several small cohorts, thus allowing a better characterization of the syndrome. It should be distinguished from other startle-associated syndromes, such as hyperekplexia, where the exaggerated startle response can lead to falls, but without other clinical manifestations nor changes in EEG [12,13]. The clinical and EEG characteristics of startled-epilepsy patients were studied in five cohorts, corresponding to 83 patients, which showed an important variability [5,8-11] (Table 1).

We reviewed literature on startle epilepsy along with the most frequent electrophysiological characteristics reported in PubMed and Google Scholar database. And searched the following keywords: startle AND epilepsy AND electrophysiology OR EEG recording. This review included papers from 1955 to 2021 (this study was conducted in 2021). We selected studies and case reports that matched our keywords and investigated further studies with large cohorts and electrophysiological data. After selecting 35 studies, most of which were isolated case reports, we focused on five cohorts reporting electro-clinical data of over ten patients [5,8-11].

Startle epilepsy usually begins between 10 months and 14 years of age [1,5,8-11,14], however a few cases of late adult-onset have been reported [5,6]. The sex ratio is balanced. It often occurs in the context of hemiparesis and brain damage secondary to ante- or neonatal hypoxia [1,5,8-11,14], and less frequently in patients with Down syndrome [15], Lennox-Gastaut or Sturge-Weber syndrome. More rarely, startle seizures can be observed in genetic lysosomal storage disorders (partylglucosaminuria, GM1 and GM2 gangliosidosis and Krabbe disease) [16] or in patients with IL1RAPL1 gene deletion [17].

Patients with neonatal brain lesions often suffer from cognitive impairment [1,5,8-11,14]. However, in the cohort of Chauvel et al. [2] and Job et al. [18] underlined that cognitive deficit is not systematic and that a proportion of patients could pursue higher education. Brain imaging reveals abnormalities like multifocal lesions or cortical atrophy (most often fronto-central or parietal) [1,5,8-11,14]. However Job et al. [18] reported a series of 3 cases without lesions on cerebral MRI nor pathology screening.

The auditory modality is the most common trigger of seizures, followed by somesthetic stimulation (most often stimulation of the paretic hemisphere) and visual stimulation. A case of seizures triggered by a strong and startling odor has been described [19]. The intensity of the stimulus which is required to trigger seizures is highly variable, depending on the patient's level of attention and anticipation. The occurrence of seizures during sleep, as in our patient, has been described (25% of patients in the cohort of Aguglia et al. [8]). The occurrence of unprovoked seizures is also quite frequent, up to 100% of patients depending on studies, and is described in the 5 cohorts [5,8-11].

There is a great heterogeneity in the ictal manifestations described in startle epilepsy. Our patient’s seizures starting with paresthesia followed by a hemi-tonic contraction, were reported in 26% of the cases in the cohort of Manford et al. [5]. Initial somesthetic manifestations could have been underestimated in the other cohorts, particularly those in which patients suffered a major cognitive impairment [10]. Literature also reports symptoms such as epigastric sensation, automatism, or urination [10]. Hemi-tonic seizures (in the paretic limbs) are the most frequent type of seizure, followed by myoclonic seizures and bilateral tonic seizures. Generalized tonic-clonic seizures are also common and may be found as frequently as tonic seizures in some studies [9]. Rarely, patients may show absence-type seizures [5,11] or atonic seizures [8]. As shown in Table 1, the distribution of clinical data according to seizures' type is variable across studies. The phenomenology of unprovoked and provoked seizures can be similar or quite distinct. In most cases, like ours, unprovoked seizures of different phenomenology can precede by years the onset of startle epilepsy. Literature is homogeneous in terms of high seizure frequency, over one seizure per day.

There are variable electro-clinical patterns of startle epilepsy described in the literature. Recent series [5,10,11] report normal interictal EEG in 45% of patients. Commonly observed interictal abnormalities include a slowing of the background rhythm, focal spikes (over frontal, centro-parietal, medial electrodes sometimes over temporal electrodes), multifocal spikes [1,5,8-11], or spike-and-slow-wave pattern [20]. Subclinical rhythmic spike discharges were also described [8,11]. In the cohort of Aguglia et al. 8 sleep recordings allowed the detection of frontal abnormal activities in all patients.

Recent cohorts focusing on ictal EEG patterns agree on the short duration of seizures, of less than 10 seconds. Like in our patient's case, focal fast rhythms are described at the onset of seizures [5,10,11,14] in 9 to 40% of cases. The most common initial pattern in these cohorts is diffuse flattening of the background rhythm (called diffuse electro-decremental pattern or DEP), present in approximately 60% of patients. Ictal EEG pattern appears as an isolated focal spike (over median, right, or left fronto-central electrodes) followed by a rhythmic localized or bilateral discharge of spikes. The representation of each ictal EEG pattern is different across the five cohorts [5,8-11]. It is important to note that EEG recording may be normal during a seizure or difficult to interpret due to muscle artifacts in 22 to 66% of cases [5,10]. In fact, identifying startle muscle artifacts can hamper the analysis of the seizure's onset.

Chauvel et al. [2] provide SEEG recordings from twenty patients with startle epilepsy. The seizure starts with an abnormally high voltage in the primary motor cortex or supplementary motor area, in the same time frame as a spike recorded in scalp EEG over the central median electrode, i.e., Cz (called "evoked spike"). This is followed by a low-voltage rapid discharge, also localized either in the primary motor cortex or in the supplementary motor area, with a propagation to the mesial cortex of the homolateral and contralateral frontal lobes. For Chauvel and colleagues, startle epilepsy seizures thus originate in the motor and premotor cortices. Other recent studies reported a seizure onset zone located in the premotor cortex [21-22], the prefrontal cortex, and anterior and middle cingulate cortex [23]. The SMA was involved in the epileptic network of the majority of cases [21-24]. Using the Epileptogenicity Maps method, Job et al. [18] identified an increase of high frequency oscillations in the premotor and prefrontal areas during startle epilepsy seizures and a constant involvement of the SMA.

Startle epilepsy is often drug-resistant. Commonly used treatments with relative efficiency include Lamotrigine [25,26], Oxcarbazepine, and benzodiazepines [8]. Vagus nerve stimulation was effective in isolated case reports [27]. Non-invasive sound generator treatment [28] could reduce 50% of seizure-frequency in two patients out of four. This device produces a background sound that does not disturb hearing but induces a relaxing mood and a feeling of control over the sound environment.

Surgery was effective in many studies [7,18,21-24,29,30]. However, the proximity to the primary motor cortex requires rigorous preoperative evaluation and the use of intracranial recordings. Different types of procedures are proposed with similar results: corpus callostomy [7,29], hemispherotomy [30] or focal resection [7,18,21-24]. In these studies, postoperative outcomes at one year (or more) were satisfactory with a majority of Engel class 1 [7,18,21-24,29,30], and showed no associated motor or cognitive deficit. Post-operative motor deficit could also rapidly improve in a few months [24]. One patient [7] had persistent myoclonic jerks several times a day but he no longer had seizures with falls and loss of consciousness. The surgery performed in this patient was a callostomy, which could explain the reduction of generalized seizures but the persistence of focal seizures.

Job et al. findings [18] underline the fact that surgery should be considered even in the absence of MRI lesions. However it is important to note that there probably is a publication bias in favor of the cases with a good response to surgery.

There are anatomical, and pathological mechanisms underlying startle epilepsy [1,2,20,31-36]. Surface EEG recordings and functional neuroimaging (fMRI, ictal SPECT, FDG PET) showed mesial fronto-parietal cortex, primary and premotor cortex, supplementary motor area, primary somesthetic cortex and precuneus involvement in the generation of seizures. Chauvel et al recorded startle epilepsy with SEEG and proposed a potential involvement of the proprioceptive transcortical loop in the startle response. The startle stimulus triggers the startle (subcortical mechanism), which generates a proprioceptive signal (through the osteoarticular and muscle receptors). This proprioceptive afferent volley projects on the somesthetic cortex and then on the motor cortex by a reflex transcortical loop, and triggers a critical motor discharge, making it more excitable. For these patients, the motor cortex is the site of neonatal lesions. This hypothesis can be defended sometimes if we identify latency between the occurrence of the "evoked spike" and the first bursts of critical muscle activity. Lamarche and Vignal [36] suggested the existence of such a transcortical loop, connecting the somesthetic afferences coming from neuromuscular spindles to the primary somesthetic cortex and the primary motor cortex. This hypothesis is supported by Bancaud’s experiments [32] on an animal model of startle epilepsy. When the animal is curarized, the seizures disappear. This also helps explain how various sensory modalities can induce startle seizures. For our patient, it is important to note that the startle response is amplified, possibly because of brain lesions associating spasticity and loss of cortical feedback control [1,2,32]. Based on functional imaging data, Fernandez et al. [33], proposed an evolutionist explanation of the existence of this transcortical loop. The startle reflex aims to prepare for a voluntary movement in response to the threat; this motor response itself requires spatial orientation information, through a somatosensory channel, to be correctly directed. Therefore, the authors hypothesize that the startle reflex would prepare the "defensive" voluntary movement in response to the stimulus, via activation of the supplementary motor area and the premotor cortex, according to the provided spatial information of the primary somatosensory areas.