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 10 for Epileptic "encephalopathy," early "infantile," 2
  1. CDKL5 deficiency disorder 
    ... encephalopathy CDKL5-related epilepsy CDKL5-related epileptic encephalopathy Early infantile epileptic encephalopathy 2 Genetic Testing Registry: Developmental and epileptic encephalopathy, 2 ...
    https://medlineplus.gov/genetics/condition/cdkl5-deficiency-disorder - Genetics
  2. KCNB1 encephalopathy 
    ... their family. Early infantile epileptic encephalopathy 26 EIEE26 Epileptic encephalopathy, early infantile, 26 KCNB1-related epilepsy Genetic Testing Registry: Developmental ...
    https://medlineplus.gov/genetics/condition/kcnb1-encephalopathy - Genetics
  3. SCN8A-related epilepsy with encephalopathy 
    ... no history of the disorder in their family. Early infantile epileptic encephalopathy 13 EIEE13 SCN8A encephalopathy Genetic Testing Registry: Developmental ...
    https://medlineplus.gov/...cn8a-related-epilepsy-with-encephalopathy - Genetics
  4. SLC35A2-congenital disorder of glycosylation 
    ... CDGIIm Congenital disorder of glycosylation, type IIm EIEE22 Epileptic encephalopathy, early infantile, 22 SLC35A2-CDG Genetic Testing Registry: SLC35A2-congenital ...
    https://medlineplus.gov/...35a2-congenital-disorder-of-glycosylation - Genetics
  5. STXBP1 encephalopathy 
    ... encephalopathy 4 Developmental and epileptic encephalopathy, type 4 Early-infantile epileptic encephalopathy 4 EIEE4 STXBP1 encephalopathy with epilepsy STXBP1 epileptic ...
    https://medlineplus.gov/genetics/condition/stxbp1-encephalopathy - Genetics
  6. Malignant migrating partial seizures of infancy 
    ... in embryonic development (called a de novo mutation). Early infantile epileptic encephalopathy 14 EIEE14 Malignant migrating partial epilepsy of infancy ...
    https://medlineplus.gov/...ant-migrating-partial-seizures-of-infancy - Genetics
  7. Developmental and epileptic encephalopathy 1 
    ... their sons. Early infantile epileptic encephalopathy-1 EIEE1 Epileptic encephalopathy, early infantile, 1 Infantile epileptic-dyskinetic encephalopathy ISSX ISSX1 X- ...
    https://medlineplus.gov/...elopmental-and-epileptic-encephalopathy-1 - Genetics
  8. GRIN2B-related neurodevelopmental disorder 
    ... history of the disorder in their family. EIEE27 Epileptic encephalopathy, early infantile, 27 GRIN2B encephalopathy GRIN2B related syndrome Genetic Testing ...
    https://medlineplus.gov/...rin2b-related-neurodevelopmental-disorder - Genetics
  9. Lennox-Gastaut syndrome 
    ... H, Matsumoto N. De novo DNM1 mutations in two cases of epileptic encephalopathy. ... KG. Evolution of Infantile Spasms to Lennox-Gastaut Syndrome: What Is There ...
    https://medlineplus.gov/genetics/condition/lennox-gastaut-syndrome - Genetics
  10. Infantile-onset spinocerebellar ataxia 
    ... L, Pihko H. Recessive twinkle mutations cause severe epileptic encephalopathy. Brain. 2009 Jun;132(Pt 6):1553-62. doi: 10.1093/brain/awp045. Epub 2009 Mar 20. Citation on PubMed Lonnqvist T. Infantile-Onset Spinocerebellar Ataxia. 2009 Jan 27 [updated 2018 ...
    https://medlineplus.gov/.../infantile-onset-spinocerebellar-ataxia - Genetics