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Results 11 - 20 of 70 for Childhood epilepsy
  1. 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
  2. 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
  3. 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
  4. Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 
    ... About half of affected individuals develop recurrent seizures (epilepsy) beginning early in childhood. People with MPPH syndrome also have difficulty coordinating ...
    https://medlineplus.gov/...ogyria-polydactyly-hydrocephalus-syndrome - Genetics
  5. PRICKLE1-related progressive myoclonus epilepsy with ataxia 
    ... Although a few affected individuals have died in childhood, many have lived into adulthood. The prevalence of PRICKLE1-related progressive myoclonus epilepsy with ataxia is unknown. The condition has been ...
    https://medlineplus.gov/...rogressive-myoclonus-epilepsy-with-ataxia - Genetics
  6. DLG4-related synaptopathy 
    ... of individuals with this condition have recurrent seizures (epilepsy) that typically begin in childhood. Brain changes can also occur. These include brain ...
    https://medlineplus.gov/genetics/condition/dlg4-related-synaptopathy - Genetics
  7. 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
  8. Short-chain acyl-CoA dehydrogenase deficiency 
    ... deficiency in the Netherlands, but no association with epilepsy of unknown origin in childhood. Neuropediatrics. 2011 Feb;42(1):13-7. doi: ...
    https://medlineplus.gov/...t-chain-acyl-coa-dehydrogenase-deficiency - Genetics
  9. Infantile-onset spinocerebellar ataxia 
    ... nerve damage (sensorineural hearing loss) typically occurs during childhood and progresses to profound deafness.Individuals with IOSCA may have recurrent seizures (epilepsy). These seizures can lead to severe brain dysfunction ( ...
    https://medlineplus.gov/.../infantile-onset-spinocerebellar-ataxia - Genetics
  10. Spinal muscular atrophy with progressive myoclonic epilepsy 
    ... PME) is a neurological condition that begins in childhood. SMA-PME causes muscle weakness and wasting (atrophy) and a combination of seizures and uncontrollable muscle jerks (myoclonic epilepsy).In individuals with SMA-PME, spinal muscular atrophy ...
    https://medlineplus.gov/...rophy-with-progressive-myoclonic-epilepsy - Genetics
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