Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 17 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. GABRA1 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Childhood absence epilepsy More About This Health Condition ECA4 EJM EJM5 ...
    https://medlineplus.gov/genetics/gene/gabra1 - Genetics
  3. EFHC1 gene 
    ... juvenile myoclonic epilepsy. This condition typically begins in childhood ... myoclonic epilepsy replace single protein building blocks (amino acids) in ...
    https://medlineplus.gov/genetics/gene/efhc1 - Genetics
  4. 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
  5. 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
  6. 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
  7. SCN9A gene 
    ... characterized by convulsive seizures in infancy, followed in childhood by absence seizures, which cause loss of consciousness for short periods. In mid-childhood, the seizures change to the generalized tonic-clonic ...
    https://medlineplus.gov/genetics/gene/scn9a - Genetics
  8. 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
  9. 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
  10. 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
previous · 1 · 2 · next