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16 Possible Causes for Parietal Focal Spikes, Paroxysmal Activity - Spikes Central Bilaterally, Paroxysmal Activity - Spikes Temporal Bilaterally

  • Benign Adult Familial Myoclonic Epilepsy

    […] childhood epilepsy with centrotemporal spike -childhood epilepsy with occipital paroxysms Generalized epilepsies & synd.[enotes.tripod.com] Between these bursts are inserted periods of variable duration without obvious paroxysmal discharges but with θ–wave activity of variable amplitude involving both central[neupsykey.com] , partial) seizure: Symptomatic: -temporal lobe epilepsy -frontal lobe epilepsy -parietal lobe epilepsy -occipital lobe epilepsy Idiopathic with age-related onset: -benign[enotes.tripod.com]

  • Epilepsy

    Contemporary drug therapy fails to control epileptic seizures in some 30% of patients, resulting in the need to employ other measures when they appear practicable. A good deal of potentially relevant statistical detail is available regarding the outcomes of the available antiepileptic therapies, but its interpretation[…][dx.doi.org]

  • Generalized Clonic or Tonic-Clonic Seizures

    ‘Contrary to popular folk belief, nothing should be placed in the mouth during the seizure. Severe injury could occur.’ Generalized tonic clonic seizures (grand mal seizures) are the most common and best known type of generalized seizure. They begin with stiffening of the limbs (the tonic phase), followed by jerking[…][epilepsynw.org]

  • Juvenile Myoclonic Epilepsy

    Juvenile myoclonic epilepsy is a common form of epilepsy mainly characterized by myoclonic jerks, but affected individuals may also experience generalized tonic-clonic seizures and absence seizures. Symptom onset typically occurs around puberty and although the disease persists into adulthood, patients do respond[…][symptoma.com]

  • West Syndrome

    IARS2 encodes isoleucine-tRNA synthetase, which is aclass-1 amino acyl-tRNA synthetase. IARS2 mutations are reported to cause Leigh syndrome or cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysphasia syndrome (CAGSSS). To our knowledge, IARS2 mutations and[…][ncbi.nlm.nih.gov]

  • Idiopathic Generalized Epilepsy

    Tonic status epilepticus (TSE) in patients with idiopathic generalized epilepsy (IGE) is not well recognized. The objective of this study is to report episodes of TSE in patients with IGE. We retrospectively reviewed the clinical and EEG evaluation of three IGE patients who presented TSE. The three patients had mainly[…][ncbi.nlm.nih.gov]

  • Organic Brain Syndrome

    Abstract This study addresses the prevalence of organic brain syndrome (OBS) among long-term toluene-exposed rotagravure workers who are still working. The prevalence of OBS in 22 workers exposed to toluene for a minimum of 12 years and 19 unexposed control subjects, matched for age and employment status,[…][ncbi.nlm.nih.gov]

  • Encephalopathy

    Posterior reversible encephalopathy syndrome is an encephalopathy that can be clinically characterized by headache, altered mental status and/or seizures. Neuroimaging demonstrates usually reversible bilateral subcortical vasogenic occipital-parietal edema. Exact pathophysiology remains unclear but is commonly[…][ncbi.nlm.nih.gov]

  • Juvenile Absence Epilepsy

    PURPOSE: The aim of this study to evaluate the hippocampal, frontal and thalamic lobe functions in the early stage of the juvenile absence epilepsy (JAE) by magnetic resonance proton spectroscopy (MRS). METHOD: Fourteen patients with juvenile absence epilepsy with typical absence seizures and 10 healthy volunteer[…][ncbi.nlm.nih.gov]

  • Uremic Encephalopathy

    BACKGROUND AND PURPOSE: Uremic encephalopathy is a metabolic disorder in patients with renal failure. The purpose of this study was to describe the MR imaging findings of uremic encephalopathy. MATERIALS AND METHODS: This study retrospectively reviewed MR imaging findings in 10 patients with clinically proved uremic[…][ncbi.nlm.nih.gov]