Seizure

Subjective sleep disturbances are more often seen in people with epilepsy (PWE) than in healthy controls. Questionnaire-based studies in specialized epilepsy clinics suggest that more than a third of adults with refractory epilepsy have a sleep disturbance, twice as often as in controls1,2. In children with epilepsy, the prevalence of sleep disturbances is even higher, being ten times that of classmates of the same age without epilepsy3. In the general community, the prevalence of obstructive sleep apnea syndrome (OSAS) is ...

Intracranial hemorrhage (ICH) is one of the most devastating forms of stroke with a reported mortality rate of up to 50% in the literature. [1] One complication is the development of seizures that occurs in 2%-40% of patients post-ICH. The significant variation in incidence is related to the type and duration of monitoring, length of follow-up, and patient characteristics including hemorrhage volume, hemorrhage location, and cortical involvement [2–12].

Progressive myoclonus epilepsy (PME) comprises a group of rare heterogeneous genetic disorders that are generally manifested as a combination of myoclonic and tonic-clonic seizures with cognitive impairment, ataxia and other cerebellar signs, and other neurologic deficits. They are often encompassed under the broader term “catastrophic epilepsies”, which are invariably associated with significant neurological morbidity and often early mortality. This group also include epileptic encephalopathies [1].

Sociocultural attitudes continue to have a negative impact on the management of epilepsy in many African countries, including Nigeria [1]. The disorder is negatively affected by superstition, discrimination and stigma [2]. Religion as well as socio-cultural beliefs influences the nature of treatment and care received by people with epilepsy. It is believed that epilepsy results from witchcraft or possession by evil spirits and therefore treatment should be through the use of herbs from traditional doctors, fetish priests and religious leaders.

Perampanel (PER), one of the newer antiepileptic drugs has a novel antiseizure mechanism acting as a non-competitive α-amino-3-hydroxy-5-methyl-4-isoxazole-propionic acid (AMPA) receptor antagonist [1]. It was licensed as add-on medication for refractory focal-onset seizures after conduction of 3 phase III double-blinded randomized clinical trials [2–4] followed by an open label extension with a follow-up reaching 4 years [5]. The initial clinical trials had a 6 week titration period and a 13 week follow-up period and showed high retention rates varying from ...

Focal impaired awareness seizure (FIAS) is a clinical phenomenon with a prevalence of 0.8% that manifests as epileptic discharges commonly located in the amygdala-hippocampal complex. It can cause visual delusions and olfactory, auditory, or affective hallucinations [1]. Obstructive sleep apnea (OSA) is common in patients with epilepsy [2]. Despite their limitations, some studies have revealed an important relationship between OSA and refractory epileptic seizures (RES), as well as between OSA improvement and a corresponding RES improvement with adequate continuous positive ...

We read with great interest the systematic review by Spencer et al. [1] regarding the risk factors for the development of seizures after cranioplasty in patients that sustained traumatic brain injury. The authors have revealed a pooled incidence and risk factors of post-cranioplasty seizures (PCS). We really appreciate the interesting review for their conclusion, it’s very useful to have a better understanding of PCS. However, after reading this article, we would like to highlight 2 important questions that it raises.

Unverricht―Lundborg disease (ULD) is a type of autosomal recessive progressive myoclonus epilepsy (PME). The molecular basis for ULD involves mutations in the gene encoding cystatin B, a cysteine protease inhibitor. The gene is located on chromosome 21 at q22.3 [1]. This mutation leads to the multiplication of the C4GC4GCG minisatellite sequence repeats. The normal range of repeats is 2―3, with a premutation range of 12―17, and a causative disease range of 30―80 repeats. However, the number of repeats does not ...

Eyelid myoclonia with absences (EMA) is an epileptic syndrome characterized by a well-defined clinical and electroencephalographic (EEG) phenotype: eyelid myoclonia with or without absences, eye closure-induced EEG paroxysms and photosensitivity [1].

We read with great interest the study by Shih et al [1] regarding the risk factors for seizures after cranioplasty. The article is well written and the authors have concluded that delayed cranioplasty procedures and seizures before cranioplasty were significantly associated with early post-cranioplasty seizures. We really appreciate the interesting research for their conclusion would believe it to be useful to make a treatment decision and prevent seizures in advance in cranioplasty patients. However, after reading this article, we would ...