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Results 1 - 10 of 14 for Childhood absence epilepsy
  1. Childhood absence epilepsy 
    Childhood absence epilepsy is a condition characterized by recurrent seizures (epilepsy). This condition begins in childhood, usually between ages 3 and 8. Affected ...
    https://medlineplus.gov/.../condition/childhood-absence-epilepsy - Genetics
  2. CHD2 myoclonic encephalopathy 
    ... epilepsy), abnormal brain function (encephalopathy), and intellectual disability. ... (absence seizures); seizures brought on by high body temperature ( ...
    https://medlineplus.gov/.../condition/chd2-myoclonic-encephalopathy - Genetics
  3. Genetic epilepsy with febrile seizures plus 
    ... called Dravet syndrome (also known as severe myoclonic epilepsy of infancy or ... or absence seizures. In Dravet syndrome, these seizures are difficult ...
    https://medlineplus.gov/...netic-epilepsy-with-febrile-seizures-plus - Genetics
  4. Epilepsy-aphasia spectrum 
    ... dyspraxia (ADRESD), intermediate epilepsy-aphasia disorder (IEAD), atypical childhood epilepsy with centrotemporal spikes (ACECTS), and childhood epilepsy with ...
    https://medlineplus.gov/genetics/condition/epilepsy-aphasia-spectrum - Genetics
  5. Lennox-Gastaut syndrome 
    ... during sleep.In people with Lennox-Gastaut syndrome, epilepsy begins in early childhood, usually between ages 3 and 5. The most ... Selmer KK. CHD2 mutations in Lennox-Gastaut syndrome. Epilepsy Behav. 2014 Apr;33:18-21. doi: ... of infancy and childhood. Lancet Neurol. 2016 Mar;15(3):304-16. ...
    https://medlineplus.gov/genetics/condition/lennox-gastaut-syndrome - Genetics
  6. Juvenile myoclonic epilepsy 
    ... epilepsy is a condition characterized by recurrent seizures (epilepsy). This condition begins in childhood or adolescence, usually between ages 12 and 18, ...
    https://medlineplus.gov/.../condition/juvenile-myoclonic-epilepsy - Genetics
  7. STXBP1 encephalopathy 
    ... begin in infancy but can start later in childhood or early adulthood. In many affected individuals who have epilepsy, the seizures stop after a few years, and ...
    https://medlineplus.gov/genetics/condition/stxbp1-encephalopathy - Genetics
  8. 15q11-q13 duplication syndrome 
    ... death during sleep (called sudden unexpected death in epilepsy, or SUDEP).Hearing loss in childhood is common in dup15q syndrome and usually results ...
    https://medlineplus.gov/.../condition/15q11-q13-duplication-syndrome - Genetics
  9. Beta-propeller protein-associated neurodegeneration 
    ... disease.Many people with BPAN have recurrent seizures (epilepsy) beginning in infancy or early childhood. Several different types of seizures can occur in ...
    https://medlineplus.gov/...ller-protein-associated-neurodegeneration - Genetics
  10. Christianson syndrome 
    ... do learn to walk lose the ability in childhood. Most affected children also have recurrent seizures (epilepsy), beginning between ages 1 and 2.Other features ...
    https://medlineplus.gov/genetics/condition/christianson-syndrome - Genetics
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