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Results 1 - 7 of 7 for "Childhood-onset" epilepsy syndrome
  1. Curing the Epilepsies: The Promise of Research From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Epilepsy/Statistics and Research ... Epilepsy ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health ... Request free mailed ...
    https://www.ninds.nih.gov/.../curing-epilepsies-promise-research - External Health Links
  2. Polymicrogyria 
    ... Ohta H, Abiru K, Nakano K, Oka E. Childhood-onset epilepsy associated with ... Lennox-Gastaut syndrome, and GPR56 gene mutations. Epilepsia. 2009 Jun;50( ...
    https://medlineplus.gov/genetics/condition/polymicrogyria - Genetics
  3. GLUT1 deficiency syndrome 
    ... Vincent A, Wilson M. Incidence and phenotypes of childhood-onset genetic ... Transporter Type 1 Deficiency Syndrome. 2002 Jul 30 [updated 2018 Mar 1]. In: ...
    https://medlineplus.gov/genetics/condition/glut1-deficiency-syndrome - Genetics
  4. CDKL5 deficiency disorder 
    ... Vincent A, Wilson M. Incidence and phenotypes of childhood-onset genetic epilepsies: a prospective population-based national cohort. Brain. 2019 ...
    https://medlineplus.gov/genetics/condition/cdkl5-deficiency-disorder - Genetics
  5. Myoclonic epilepsy with ragged-red fibers 
    ... family history of MERRF. Fukuhara disease MERRF MERRF syndrome Myoclonic epilepsy associated with ragged-red fibers Myoencephalopathy ragged-red fiber disease Genetic Testing Registry: MERRF syndrome MERRF ... MYOCLONIC EPILEPSY ASSOCIATED WITH RAGGED-RED FIBERS; MERRF PubMed Blakely ...
    https://medlineplus.gov/...myoclonic-epilepsy-with-ragged-red-fibers - Genetics
  6. Dentatorubral-pallidoluysian atrophy 
    ... person's mother (maternal inheritance). DRPLA Haw River syndrome Myoclonic epilepsy with choreoathetosis Naito-Oyanagi disease NOD Genetic Testing Registry: Dentatorubral-pallidoluysian atrophy Dentatorubral pallidoluysian atrophy ... Roses AD, Lee JE, Hulette C, Pericak-Vance MA, Vance JM. The Haw River syndrome: dentatorubropallidoluysian atrophy (DRPLA) in an African-American family. ...
    https://medlineplus.gov/.../dentatorubral-pallidoluysian-atrophy - Genetics
  7. Familial paroxysmal kinesigenic dyskinesia 
    ... infantile convulsions and choreoathetosis (ICCA) and ICCA-related syndromes. J Med Genet. ... paroxysmal kinesigenic dyskinesia with PRRT2 gene mutations. Dev ...
    https://medlineplus.gov/...amilial-paroxysmal-kinesigenic-dyskinesia - Genetics