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214 Possible Causes for Astrocytic Gliosis, Epilepsy

  • Status Epilepticus

    Pathologic findings of the gyrus around the tumor revealed mild gliosis with proliferating astrocytes but no evidence of glioma.[] We report the first case of epilepsy surgery in a liver-transplanted patient with refractory temporal lobe epilepsy.[] In both fields of epilepsy and status epilepticus, the most frequently cited journal was Epilepsia (26 articles on epilepsy and 19 articles on status epilepticus).[]

  • Chronic Fatigue Syndrome

    PubMed Google Scholar Hwang SY, Jung JS, Kim TH, Lim SJ, Oh ES, Kim JY, Ji KA, Joe EH, Cho KH, Han IO: Ionizing radiation induces astrocyte gliosis through microglia activation[] Virus in brain of child with hemiplegia, hemiconvulsions, and epilepsy. Lancet. 1977; 2 666 63 Walter G F, Renella R R.[] Vicky Whittemore is an epilepsy researcher recently tasked with overseeing CFS-ME research at the National Institute of Neurological Disorders and Stroke, and a member of[]

  • Medial Sclerosis

    Microscopic features are decrease in hippocampal neurons and gliosis.[] Mesial temporal sclerosis can cause a type of epilepsy called temporal lobe epilepsy.[] In the majority of cases, there may be no cause that can be discovered for epilepsy.[]

  • Rasmussen Syndrome

    […] loss and gliosis of the affected hemisphere 9, 10.[] Febrile infection-related epilepsy syndrome (FIRES) may also have an immune basis, although this is yet to be proven.[] If you would like to know more about epilepsy in general, please contact Epilepsy Action.[]

  • Epilepsy

    Astrocyte reactivity Evidence suggests that the BBB disruption contributes to astrocyte activation and gliosis.[] […] childhood Seizure syndrome Seizure prediction Mirgi Idiopathic epilepsy Secondary epilepsy Symptomatic epilepsy Saint Valentine's Malady Intractable epilepsy epilepsy syndrome[] The symptoms of epilepsy usually vary on the basis of underlying pathology. Seizure is the only symptom which is present in all types of epilepsy.[]

  • Cerebral Palsy

    The cerebellar white matter showed astrocytic gliosis, vacuolation of the neuropil and a diffuse infiltrate mainly of T-lymphocytes.[] We describe the first clinical case with a 1.607 Mb duplication at 3q29 (chr3: 195,731,956-197,339,329), accompanied by severe intellectual disability, epilepsy, and cerebral[] […] patient showed no midbrain-hypothalamus dysplasia or congenital/postnatal microcephaly, but dyskinetic cerebral palsy and severe intellectual disability as well as multifocal epilepsy[]

  • Lafora Disease

    As shown in Figure 4A , immunostaining showed a significant reduction in the number of Gfap-positive astrocytes in the brains sections of the double mutants as compared to[] Four children are described with progressive myoclonus epilepsy and intellectual deterioration in whom this diagnosis was made.[] Minassian and Subramaniam Ganesh, Gene defects in progressive myoclonus epilepsy, Epilepsia, 51, (75), (2010). A.C.[]

  • McLeod Neuroacanthocytosis Syndrome

    Marked neuronal loss and astrocytic gliosis were observed on histologic examination.[] Familial temporal lobe epilepsy as a presenting feature of choreoacanthocytosis. Epilepsia. 2005;46(8):1256-63.[] A cell loss of 90% in the striatum with astrocytic gliosis has been reported.[]

  • Alpers Syndrome

    The prognosis is poor and most children die in the first decade of life mainly due to intractable epilepsy.[] The neuropathology of vCJD is characteristic with grey matter spongiform degeneration, reactive astrocytic gliosis, and “florid plaques” which are pathognomonic of vCJD.[] The patient died in early childhood of fulminant hepatic failure, refractory epilepsy, lactic acidemia, and coma. mtDNA content was 30% of normal in skeletal muscle and 25%[]

  • Dentatorubral-Pallidoluysian Atrophy

    […] a patient with a possible metabolic epilepsy[] The globus pallidus (lateral greater than medial segment) and subthalamic nucleus demonstrate consistent neuronal loss and astrocytic gliosis.[] DISCUSSION: Partial seizure is one of the common epileptic features in juvenile type DRPLA, especially in patients with younger epilepsy onset.[]

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