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Results 1 - 5 of 5 for Early infantile epileptic encephalopathy 18
  1. CDKL5 deficiency disorder 
    ... encephalopathy CDKL5-related epilepsy CDKL5-related epileptic encephalopathy Early infantile epileptic encephalopathy 2 Genetic Testing Registry: Developmental and epileptic encephalopathy, ...
    https://medlineplus.gov/genetics/condition/cdkl5-deficiency-disorder - Genetics
  2. 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
  3. Lennox-Gastaut syndrome 
    ... and phenotypes of epilepsy-associated genes in epileptic encephalopathies. Genes Brain Behav. 2018 Nov;17(8):e12456. doi: 10.1111/gbb.12456. Epub 2018 Jan 26. Citation on PubMed
    https://medlineplus.gov/genetics/condition/lennox-gastaut-syndrome - Genetics
  4. TWNK gene 
    ... Sajantila A, Lonnqvist T, Spelbrink JN, Suomalainen A. Infantile-onset ... in early onset encephalopathy with mtDNA depletion. Brain. 2007 Nov;130(Pt ...
    https://medlineplus.gov/genetics/gene/twnk - Genetics
  5. CACNA1A gene 
    ... Walsh P, Winawer MR. De novo mutations in epileptic encephalopathies. Nature. 2013 Sep 12;501(7466):217-21. ... function de novo CACNA1A mutations cause severe developmental epileptic encephalopathies in the spectrum of Lennox-Gastaut syndrome. Epilepsia. ...
    https://medlineplus.gov/genetics/gene/cacna1a - Genetics