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17 Possible Causes for Paroxysmal Activity - Spikes Parietal Left, Paroxysmal Activity - Spikes Temporal Bilaterally

  • Epilepsy

    Abstract Objectives The standardized mortality ratio for suicide in people with epilepsy is reported as 5.1 [95% confidence interval (CI): 3.9–6.6], but this is only partially explained by the high rates of psychiatric comorbidity. This issue was revived when, in 2008, the Food and Drug Administration (FDA) issued an[…][oadoi.org]

  • Generalized Clonic or Tonic-Clonic Seizures

    Abstract Clinical course and long-term seizure prognosis were studied in 155 patients with complex-partial seizures during a follow-up of 10.1 /- 1 (SD) years. In 79% of the patients generalized tonic-clonic seizures were recorded, mostly within the first 3 years of epilepsy but occurring as late as 20 years after[…][ncbi.nlm.nih.gov]

  • Benign Adult Familial Myoclonic Epilepsy

    OBJECTIVE: The pathogenesis of benign adult familial myoclonic epilepsy (BAFME) remains unknown, although cerebellar pathologic changes and brain hyperexcitability have been reported. We used resting-state functional magnetic resonance imaging (fMRI) to examine the functional connectivity between the cerebellum and[…][ncbi.nlm.nih.gov]

  • Juvenile Myoclonic Epilepsy

    Juvenile myoclonic epilepsy is a condition characterized by recurrent seizures (epilepsy). This condition begins in childhood or adolescence, usually between ages 12 and 18, and lasts into adulthood. The most common type of seizure in people with this condition is myoclonic seizures, which cause rapid, uncontrolled muscle[…][ghr.nlm.nih.gov]

  • West Syndrome

    West Syndrome is a severe epileptic encephalopathy characterized by epileptic spasms, hypsarrhythmia, and regression of psychomotor acquisitions beginning in the first year of life. ARX and CDKL5 genes were identified as linked to the most frequent genetic causes of West Syndrome. The present study reports the[…][ncbi.nlm.nih.gov]

  • Idiopathic Generalized Epilepsy

    Idiopathic generalized epilepsies (IGEs) constitute one third of all epilepsies. They are genetically determined and affect otherwise normal people of both sexes and all races. IGEs manifest with typical absences, myoclonic jerks, and generalized tonic-clonic seizures, alone or in varying combinations and severity.[…][epilepsy.com]

  • Myoclonic-Astatic Epilepsy

    Myoclonic-astatic epilepsy, also known as Doose syndrome, is a type of idiopathic childhood epilepsy presenting with astatic as well as myoclonic component. It presents in children with previously normal development but can cause some degree of mental disturbance later in life. Myoclonic-astatic epilepsy (MAE) consists[…][symptoma.com]

  • Organic Brain Syndrome

    An organic brain syndrome ( OBS ), also known as an organic brain disease/disorder ( OBD ), an organic mental syndrome ( OMS ), or an organic mental disorder ( OMD ), is a syndrome or disorder of mental function whose cause is alleged to be known as organic ( physiologic ) rather than purely of the mind. These[…][en.wikipedia.org]

  • Encephalopathy

    Eclampsia, an obstetric emergency frequently seen in pregnant or puerperal women, is a risk factor for posterior reversible encephalopathy syndrome (PRES). Most cases of eclampsia occur postpartum. We report a woman with PRES associated with eclampsia 10 weeks post-delivery, the latest onset ever reported. A[…][ncbi.nlm.nih.gov]

  • Juvenile Absence Epilepsy

    Neurol Sci. 2016 Feb;37(2):289-92. doi: 10.1007/s10072-015-2411-y. Epub 2015 Nov 3. Author information 1 Neurosciences Research Center, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran. aliasadipooya@yahoo.com. 2 Department of Neurology, Jefferson Comprehensive Epilepsy Center, Thomas Jefferson[…][ncbi.nlm.nih.gov]

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