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Results 1 - 10 of 14 for "Epilepsy," childhood absence 2
  1. Childhood absence epilepsy 
    ... mal epilepsy Pykno-epilepsy Pyknolepsy Genetic Testing Registry: Epilepsy, childhood absence 2 Genetic Testing Registry: Epilepsy, childhood absence 4 Genetic ...
    https://medlineplus.gov/.../condition/childhood-absence-epilepsy - 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 seen in many people with Christianson ...
    https://medlineplus.gov/genetics/condition/christianson-syndrome - Genetics
  3. 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
  4. 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
  5. Epilepsy-aphasia spectrum 
    ... and definition of epilepsy syndromes with onset in childhood: Position paper by the ... spectrum. Epilepsia. 2013 Feb;54(2):280-7. doi: 10.1111/epi.12065. Epub ...
    https://medlineplus.gov/genetics/condition/epilepsy-aphasia-spectrum - Genetics
  6. Lennox-Gastaut syndrome 
    ... during sleep.In people with Lennox-Gastaut syndrome, epilepsy begins in early childhood, usually between ages 3 and 5. The most ... for 3 to 4 percent of cases of epilepsy in children and 1 to 2 percent of cases in adults. For unknown reasons, ...
    https://medlineplus.gov/genetics/condition/lennox-gastaut-syndrome - 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. 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
  9. 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 ... isodicentric chromosome 15 syndrome: The role of SUDEP. Epilepsy Behav. 2016 ... genomic disorders of chromosome 15q11.2-q13. Neurobiol Dis. 2010 May;38(2):181- ...
    https://medlineplus.gov/.../condition/15q11-q13-duplication-syndrome - Genetics
  10. Spinal muscular atrophy with progressive myoclonic epilepsy 
    Spinal muscular atrophy with progressive myoclonic epilepsy (SMA-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 ...
    https://medlineplus.gov/...rophy-with-progressive-myoclonic-epilepsy - Genetics
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