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Results 1 - 4 of 4 for Epileptic "encephalopathy," infantile or early "childhood," 3
  1. SLC35A2-congenital disorder of glycosylation 
    ... typically develop signs and symptoms of the condition early in infancy. Seizures ... unusual facial features, skeletal abnormalities, and weak muscle ...
    https://medlineplus.gov/...35a2-congenital-disorder-of-glycosylation - Genetics
  2. CDKL5 deficiency disorder 
    ... encephalopathy CDKL5-related epilepsy CDKL5-related epileptic encephalopathy Early infantile epileptic encephalopathy 2 ... T. CDKL5-Related Disorders: From Clinical Description to Molecular Genetics. Mol Syndromol. 2012 Apr;2(3-5):137-152. doi: 10.1159/000331333. Epub ...
    https://medlineplus.gov/genetics/condition/cdkl5-deficiency-disorder - Genetics
  3. 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
  4. Lennox-Gastaut syndrome 
    ... during sleep.In people with Lennox-Gastaut syndrome, epilepsy begins in early childhood, usually between ages 3 and 5. The most common seizure type is ...
    https://medlineplus.gov/genetics/condition/lennox-gastaut-syndrome - Genetics