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Results 1 - 10 of 20 for Myoclonic epilepsy in infancy
Did you mean mayoclinic epilepsy in infancy?
  1. SCN1A gene 
    ... such as Dravet syndrome (also known as severe myoclonic epilepsy of infancy or SMEI), that cause more serious seizures that ... Clinical spectrum of mutations in SCN1A gene: severe myoclonic epilepsy in infancy and related epilepsies. Epilepsy Res. 2006 Aug;70 ...
    https://medlineplus.gov/genetics/gene/scn1a - Genetics
  2. Genetic epilepsy with febrile seizures plus 
    ... condition called Dravet syndrome (also known as severe myoclonic epilepsy of infancy or SMEI) is often considered part of the GEFS+ spectrum and is the most severe disorder in this group. Affected ... include myoclonic or absence seizures. In Dravet syndrome, these seizures ...
    https://medlineplus.gov/...netic-epilepsy-with-febrile-seizures-plus - Genetics
  3. Seizures (National Library of Medicine)  
    Seizures are symptoms of a brain problem. They happen because of sudden, abnormal electrical activity in the brain. When people think of seizures, they often ...
    https://medlineplus.gov/seizures.html - Health Topics
  4. Epilepsy (National Library of Medicine)  
    Epilepsy is a brain disorder that causes people to have recurring seizures. The seizures happen when clusters of nerve cells, or neurons, in the brain send out ...
    https://medlineplus.gov/epilepsy.html - Health Topics
  5. Juvenile myoclonic epilepsy 
    ... several members of a large family with juvenile myoclonic epilepsy. The GABRA1 gene ... After infancy, the influx of chloride ions creates an environment ...
    https://medlineplus.gov/.../condition/juvenile-myoclonic-epilepsy - Genetics
  6. Epilepsy and Seizures From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Epilepsy/Start Here ... Epilepsy ... Seizures/Start Here ... Seizures ... National Institute of Neurological Disorders and Stroke ... Epilepsy is a chronic brain disorder in which ...
    https://www.ninds.nih.gov/.../disorders/epilepsy-and-seizures - External Health Links
  7. SCN8A-related epilepsy with encephalopathy 
    ... and symptoms of this condition typically begin in infancy.The seizures in ... (myoclonic seizures), or loss of consciousness with muscle rigidity ...
    https://medlineplus.gov/...cn8a-related-epilepsy-with-encephalopathy - Genetics
  8. GABRA1 gene 
    ... identified in at least one family with juvenile myoclonic epilepsy. This condition typically begins in childhood or adolescence ... GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy. Nat Genet. 2002 Jun;31(2):184-9. ...
    https://medlineplus.gov/genetics/gene/gabra1 - Genetics
  9. Cerebral folate transport deficiency 
    ... A, Cormand B, Artuch R. Progressive ataxia and myoclonic epilepsy in a patient with a homozygous mutation in ...
    https://medlineplus.gov/.../cerebral-folate-transport-deficiency - Genetics
  10. Dentatorubral-pallidoluysian atrophy 
    ... s mother (maternal inheritance). DRPLA Haw River syndrome Myoclonic epilepsy with choreoathetosis Naito-Oyanagi disease NOD Genetic Testing ...
    https://medlineplus.gov/.../dentatorubral-pallidoluysian-atrophy - Genetics
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