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Results 1 - 6 of 6 for Developmental epileptic "encephalopathy," 70
  1. Developmental and epileptic encephalopathy 1 
    ... National Organization for Rare Disorders (NORD) ... new paradigm for West syndrome based on molecular and cell biology. Epilepsy Res. 2006 Aug;70 Suppl 1:S87-95. doi: 10.1016/j. ...
    https://medlineplus.gov/...elopmental-and-epileptic-encephalopathy-1 - Genetics
  2. Epilepsy-aphasia spectrum 
    ... family. Acquired aphasia with epilepsy DEE/EE-SWAS Developmental and/or epileptic encephalopathy with spike-wave activation in Sleep Epilepsy with ...
    https://medlineplus.gov/genetics/condition/epilepsy-aphasia-spectrum - Genetics
  3. Lennox-Gastaut syndrome 
    ... mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies. Am J Hum Genet. 2014 Oct 2;95(4):360-70. doi: 10.1016/j.ajhg.2014.08.013. ...
    https://medlineplus.gov/genetics/condition/lennox-gastaut-syndrome - Genetics
  4. 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 ... Curing the Epilepsies: ...
    https://www.ninds.nih.gov/.../curing-epilepsies-promise-research - External Health Links
  5. GLUT1 deficiency syndrome 
    ... than the common form. People with the non-epileptic form do not have seizures, but they may still have developmental delay and intellectual disability. Most have movement problems ...
    https://medlineplus.gov/genetics/condition/glut1-deficiency-syndrome - Genetics
  6. PURA syndrome 
    ... syndrome is a rare condition affecting at least 70 individuals. It is estimated to account for fewer than 1 percent of cases of developmental delay. PURA syndrome is caused by mutations in ...
    https://medlineplus.gov/genetics/condition/pura-syndrome - Genetics