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Results 1 - 5 of 5 for "Lennox-Gastaut" syndrome
  1. Lennox-Gastaut syndrome 
    Lennox-Gastaut syndrome is a severe condition characterized by repeated seizures (epilepsy) that begin early in life. Affected individuals ...
    https://medlineplus.gov/genetics/condition/lennox-gastaut-syndrome - Genetics
  2. Beta-propeller protein-associated neurodegeneration 
    ... in epileptic syndromes, such as West syndrome or Lennox-Gastaut syndrome.Children with BPAN also have intellectual disability, delayed ...
    https://medlineplus.gov/...ller-protein-associated-neurodegeneration - Genetics
  3. Polymicrogyria 
    ... T, Walsh CA, Guerrini R. Bilateral frontoparietal polymicrogyria, Lennox-Gastaut syndrome, and GPR56 gene mutations. Epilepsia. 2009 Jun;50( ...
    https://medlineplus.gov/genetics/condition/polymicrogyria - Genetics
  4. CHD2 myoclonic encephalopathy 
    ... AM, Rosby O, Selmer KK. CHD2 mutations in Lennox-Gastaut syndrome. Epilepsy Behav. 2014 Apr;33:18-21. doi: ...
    https://medlineplus.gov/.../condition/chd2-myoclonic-encephalopathy - Genetics
  5. 15q11-q13 duplication syndrome 
    ... difficult-to-treat (intractable) seizure patterns such as Lennox-Gastaut syndrome. Seizures can lead to falls, loss of developmental ...
    https://medlineplus.gov/.../condition/15q11-q13-duplication-syndrome - Genetics