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 12 for "Epilepsy," childhood absence 4
  1. Childhood absence epilepsy 
    ... mal epilepsy Pykno-epilepsy Pyknolepsy Genetic Testing Registry: Epilepsy, childhood absence 4 Genetic Testing Registry: Epilepsy, childhood absence, JRK related ...
    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. 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
  4. EFHC1 gene 
    ... a small number of people with juvenile myoclonic epilepsy. This condition ... absence seizures. Most gene mutations associated with juvenile myoclonic ...
    https://medlineplus.gov/genetics/gene/efhc1 - Genetics
  5. RAB18 deficiency 
    ... weak muscle tone (hypotonia) in infancy. By early childhood, they develop ... seizures (epilepsy).Some people with Warburg micro syndrome have reduced ...
    https://medlineplus.gov/genetics/condition/rab18-deficiency - Genetics
  6. SCN9A gene 
    ... characterized by convulsive seizures in infancy, followed in childhood by absence seizures, which cause loss of consciousness for short ... channel excited to play a role in human epilepsies. Clin Genet. 2010 Apr;77(4):326-8. doi: 10.1111/j.1399-0004. ...
    https://medlineplus.gov/genetics/gene/scn9a - Genetics
  7. Lennox-Gastaut syndrome 
    ... during sleep.In people with Lennox-Gastaut syndrome, epilepsy begins in early childhood, usually between ages 3 and 5. The most ... people worldwide. This condition accounts for 3 to 4 percent of cases of epilepsy in children and 1 to 2 percent of ...
    https://medlineplus.gov/genetics/condition/lennox-gastaut-syndrome - Genetics
  8. STXBP1 encephalopathy 
    ... epileptic encephalopathy, type 4 Early-infantile epileptic encephalopathy 4 EIEE4 STXBP1 encephalopathy with epilepsy STXBP1 epileptic encephalopathy STXBP1-related developmental and epileptic ...
    https://medlineplus.gov/genetics/condition/stxbp1-encephalopathy - 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. 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 ... region. J Autism Dev Disord. 2007 Apr;37(4):694-702. doi: 10.1007/s10803-006-0225-8. ... pain insensitivity in Dup15q. Epilepsy Behav. 2016 Feb;55:124-7. doi: 10. ...
    https://medlineplus.gov/.../condition/15q11-q13-duplication-syndrome - Genetics
previous · 1 · 2 · next