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 Myoclonic epilepsy in infancy
Did you mean mayoclinic epilepsy in infancy?
  1. Genetic epilepsy with febrile seizures plus 
    ... condition called Dravet syndrome (also known as severe myoclonic epilepsy of infancy or SMEI) is often considered part of the GEFS+ spectrum and is the most severe disorder in this group. Affected ... include myoclonic or absence seizures. In Dravet syndrome, these seizures ...
    https://medlineplus.gov/...netic-epilepsy-with-febrile-seizures-plus - Genetics
  2. Juvenile myoclonic epilepsy 
    ... several members of a large family with juvenile myoclonic epilepsy. The GABRA1 gene ... After infancy, the influx of chloride ions creates an environment ...
    https://medlineplus.gov/.../condition/juvenile-myoclonic-epilepsy - Genetics
  3. SCN8A-related epilepsy with encephalopathy 
    ... and symptoms of this condition typically begin in infancy.The seizures in ... (myoclonic seizures), or loss of consciousness with muscle rigidity ...
    https://medlineplus.gov/...cn8a-related-epilepsy-with-encephalopathy - Genetics
  4. Cerebral folate transport deficiency 
    ... A, Cormand B, Artuch R. Progressive ataxia and myoclonic epilepsy in a patient with a homozygous mutation in ...
    https://medlineplus.gov/.../cerebral-folate-transport-deficiency - Genetics
  5. Dentatorubral-pallidoluysian atrophy 
    ... s mother (maternal inheritance). DRPLA Haw River syndrome Myoclonic epilepsy with choreoathetosis Naito-Oyanagi disease NOD Genetic Testing ...
    https://medlineplus.gov/.../dentatorubral-pallidoluysian-atrophy - Genetics
  6. Farber lipogranulomatosis 
    ... Farber disease and spinal muscular atrophy with progressive myoclonic epilepsy. Hum Mutat. 2020 Sep;41(9):1469-1487. ...
    https://medlineplus.gov/genetics/condition/farber-lipogranulomatosis - Genetics
  7. Spinal muscular atrophy 
    ... diseases, such as spinal muscular atrophy with progressive myoclonic epilepsy, spinal muscular atrophy with lower extremity predominance, X- ...
    https://medlineplus.gov/genetics/condition/spinal-muscular-atrophy - Genetics
  8. Lennox-Gastaut syndrome 
    ... with Lennox-Gastaut syndrome have a history of epilepsy beginning in infancy (infantile spasms) or a related condition called West ... Selmer KK. CHD2 mutations in Lennox-Gastaut syndrome. Epilepsy Behav. 2014 ... encephalopathies of infancy and childhood. Lancet Neurol. 2016 Mar;15(3): ...
    https://medlineplus.gov/genetics/condition/lennox-gastaut-syndrome - 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 ...
    https://medlineplus.gov/...ller-protein-associated-neurodegeneration - Genetics
  10. STXBP1 encephalopathy 
    ... disability. Most affected individuals also have recurrent seizures (epilepsy). The signs and symptoms of this condition typically begin in infancy but can start later in childhood or early ...
    https://medlineplus.gov/genetics/condition/stxbp1-encephalopathy - Genetics
previous · 1 · 2 · next