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Results 1 - 10 of 21 for Absence epilepsy
  1. Childhood absence epilepsy is a condition characterized by recurrent seizures (epilepsy). This condition begins in childhood, usually between ages 3 and 8. Affected ...
  2. ... experience a type of seizure called atonic-myoclonic-absence seizure, which begins with a drop of the head, followed by loss of consciousness, then rigid movements of the arms. Epilepsy can worsen, causing prolonged episodes of seizure activity ...
  3. ... infantile spasms), partial or complete loss of consciousness (absence ... with SCN8A-related epilepsy with encephalopathy have more than one type of ...
  4. ... and loss of consciousness. Sometimes, affected individuals have absence seizures, which cause loss of consciousness for a short period that appears as a staring spell. Typically, people with juvenile myoclonic epilepsy develop the characteristic myoclonic seizures in adolescence, then ...
  5. ... the brain surface is abnormally smooth with an absence (agyria) or ... recurrent seizures (epilepsy) in individuals with ILS.More than 90 percent ...
  6. ... lipoid proteinosis. Affected individuals may have recurrent seizures (epilepsy) or behavioral and neurological problems, which can include headaches, aggressive behaviors, paranoia, hallucinations, short-term memory loss, and absence of fear. These features are thought to be ...
  7. ... include a variety of types, such as atypical absence seizures, which involve short periods ... spectrum. Affected children have rolandic seizures; these ...
  8. ... variety of seizure types. In addition to myoclonic epilepsy, they may have ... can also have absence seizures, which cause loss of consciousness for a ...
  9. ... involve rigidity, convulsions, and loss of consciousness; and absence (also known as ... death in epilepsy, or SUDEP).Hearing loss in childhood is common ...
  10. ... attacks), or partial or complete loss of consciousness (absence seizures).Some individuals with KCNB1 encephalopathy do not ... EIEE26 Epileptic encephalopathy, early infantile, 26 KCNB1-related epilepsy Genetic Testing Registry: Developmental and epileptic encephalopathy, 26 ...
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