Create issue ticket

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.[hon.ch] Abstract Lafora disease (LD), also known as progressive myoclonic epilepsy-2 (EPM2), is a rare, fatal autosomal recessive disorder typically starting during adolescence in[ncbi.nlm.nih.gov] Four children are described with progressive myoclonus epilepsy and intellectual deterioration in whom this diagnosis was made.[ncbi.nlm.nih.gov]

  • 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 .[ghr.nlm.nih.gov] Abstract Juvenile myoclonic epilepsy (JME) is a common genetic epilepsy syndrome usually presenting in adolescence and characterized by myoclonic jerks, predominately in the[ncbi.nlm.nih.gov] Author information 1 Department of Psychiatry and Psychotherapy, Social Neuroscience Lab, University of Lübeck, Lübeck, Germany; Department of Child- and Adolescent Psychiatry[ncbi.nlm.nih.gov]

  • Idiopathic Generalized Epilepsy

    Clinical aspects of juvenile myoclonic epilepsy.[journal.frontiersin.org] […] 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[ncbi.nlm.nih.gov] Idiopathic generalized epilepsies (IGEs) constitute one third of all epilepsies.[epilepsy.com]

  • 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[epilepsy-london.org] Less commonly, adolescents may present with generalized tonic-clonic seizures prior to onset of absences. Treatment is usually required for life.[epilepsydiagnosis.org] PURPOSE: Conventional teaching is that juvenile myoclonic epilepsy (JME) and juvenile absence epilepsy (JAE) require lifelong antiepileptic drug (AED) treatment.[ncbi.nlm.nih.gov]

  • Myoclonic-Astatic Epilepsy

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

  • 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.[ncbi.nlm.nih.gov] Abstract Severe myoclonic epilepsy of infancy (SMEI) is a newly recognized epileptic syndrome.[ncbi.nlm.nih.gov] […] drug therapy* Epilepsies, Myoclonic/physiopathology Epilepsy, Absence/diagnosis* Epilepsy, Absence/drug therapy* Epilepsy, Absence/physiopathology Epilepsy, Generalized/diagnosis[ncbi.nlm.nih.gov]

  • Dravet Syndrome

    Myoclonic absence seizures have not previously been described.[ncbi.nlm.nih.gov] […] 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[ncbi.nlm.nih.gov] KEYWORDS: Dravet Syndrome; Epilepsy classification; Genetic epilepsy; PCDH19-related epilepsy; SCN1A[ncbi.nlm.nih.gov]

  • Lennox-Gastaut Syndrome

    Among nonsymptomatic epilepsies exhibiting several types of generalized seizures in children two syndromes were progressively identified: epilepsy with myoclonic-astatic seizures[ncbi.nlm.nih.gov] 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.[omicsonline.org] Two developed Lennox-Gastaut type syndrome, one multifocal epilepsy, and one focal epilepsy related to a radiotherapy-induced cavernous angioma.[ncbi.nlm.nih.gov]

  • Progressive Myoclonic Epilepsy Type 7

    Published on Jan 12, 2017 progressive myoclonic epilepsy 1. Dr.[slideshare.net] Keywords progressive myoclonus - epilepsy - adolescent[thieme-connect.com] […] 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[books.google.de]

  • 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.[epilepsy.com] 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[orpha.net] 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[books.google.com]

Similar symptoms