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1,705 Possible Causes for Adolescent, Epilepsies,, Myoclonic

Did you mean: adolescence, Epilepsies, myoclonus

  • Lafora Disease

    Definition: A form of stimulus sensitive myoclonic epilepsy inherited as an autosomal recessive condition.[] Abstract Lafora disease (LD), also known as progressive myoclonic epilepsy-2 (EPM2), is a rare, fatal autosomal recessive disorder typically starting during adolescence in[] Four children are described with progressive myoclonus epilepsy and intellectual deterioration in whom this diagnosis was made.[]

  • Juvenile Myoclonic Epilepsy

    Juvenile myoclonic epilepsy affects an estimated 1 in 1,000 people worldwide. Approximately 5 percent of people with epilepsy have juvenile myoclonic epilepsy .[] Abstract Juvenile myoclonic epilepsy (JME) is a common genetic epilepsy syndrome usually presenting in adolescence and characterized by myoclonic jerks, predominately in the[] Author information 1 Department of Psychiatry and Psychotherapy, Social Neuroscience Lab, University of Lübeck, Lübeck, Germany; Department of Child- and Adolescent Psychiatry[]

  • Idiopathic Generalized Epilepsy

    Clinical aspects of juvenile myoclonic epilepsy.[] […] been reported in patients with juvenile myoclonic epilepsy (JME); however, data on other syndromes of generalized idiopathic epilepsy (IGE) other than JME, especially in adolescence[] Idiopathic generalized epilepsies (IGEs) constitute one third of all epilepsies.[]

  • Juvenile Absence Epilepsy

    We are looking at brain networks involved in the clinical expression of absence epilepsy and in juvenile myoclonic epilepsy before and after treatment – using simultaneous[] Less commonly, adolescents may present with generalized tonic-clonic seizures prior to onset of absences. Treatment is usually required for life.[] PURPOSE: Conventional teaching is that juvenile myoclonic epilepsy (JME) and juvenile absence epilepsy (JAE) require lifelong antiepileptic drug (AED) treatment.[]

  • Myoclonic-Astatic Epilepsy

    ) and myoclonic-astatic epilepsy (MAE).[] Roger J, Dravet C, Bureau M, Dreifuss FE, Wolf P (1985) Epileptic syndromes in infancy, childhood and adolescence.[] […] from myoclonic-astatic epilepsy successive of myoclonic epilepsy.[]

  • Myoclonic Epilepsy of Infancy

    Rare grand mal seizures can occur during adolescence, after withdrawal of drug treatment. The psychomotor evolution is good if treatment is started early.[] Abstract Severe myoclonic epilepsy of infancy (SMEI) is a newly recognized epileptic syndrome.[] […] drug therapy* Epilepsies, Myoclonic/physiopathology Epilepsy, Absence/diagnosis* Epilepsy, Absence/drug therapy* Epilepsy, Absence/physiopathology Epilepsy, Generalized/diagnosis[]

  • Dravet Syndrome

    Myoclonic absence seizures have not previously been described.[] […] the characteristics of Dravet syndrome during infancy and young childhood, with SCN1A mutation, but nevertheless achieved seizure freedom for at least four years during adolescence[] KEYWORDS: Dravet Syndrome; Epilepsy classification; Genetic epilepsy; PCDH19-related epilepsy; SCN1A[]

  • Lennox-Gastaut Syndrome

    Among nonsymptomatic epilepsies exhibiting several types of generalized seizures in children two syndromes were progressively identified: epilepsy with myoclonic-astatic seizures[] Purpose To describe the electroclinical features of LGS in adolescents and adults. Patients and Methods The study was developed, from May 2010 to January 2011.[] Two developed Lennox-Gastaut type syndrome, one multifocal epilepsy, and one focal epilepsy related to a radiotherapy-induced cavernous angioma.[]

  • Progressive Myoclonic Epilepsy Type 7

    Published on Jan 12, 2017 progressive myoclonic epilepsy 1. Dr.[] Keywords progressive myoclonus - epilepsy - adolescent[] […] female epilepsy patient New final section covers the epilepsy spectrum, with new chapters on epilepsy and sleep, co-morbidities of childhood, behavioral influence of AEDs[]

  • Unverricht-Lundborg Syndrome

    What is a myoclonic seizure? Myoclonic (MY-o-KLON-ik) seizures are brief, shock-like jerks of a muscle or a group of muscles.[] 1 Progressive myoclonic epilepsy type 1 Progressive myoclonus epilepsy type 1 ULD Prevalence: 1-9 / 1 000 000 Inheritance: Autosomal recessive Age of onset: Childhood , Adolescent[] Many of the genes that have been implicated in idiopathic epilepsies code for ion channels, whereas a wide spectrum of syndromes where epilepsy is a main clinical feature[]

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