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Results 1 - 6 of 6 for Epileptic "encephalopathy," infantile or early "childhood," 2
  1. CDKL5 deficiency disorder 
    ... encephalopathy Cyclin-dependent kinase-like 5 deficiency disorder Early infantile epileptic encephalopathy 2 Genetic Testing Registry: Developmental and epileptic encephalopathy, 2 ...
    https://medlineplus.gov/genetics/condition/cdkl5-deficiency-disorder - Genetics
  2. 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
  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. 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
  5. 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
  6. Infantile-onset spinocerebellar ataxia 
    ... deafness.Individuals with IOSCA may have recurrent seizures (epilepsy). These ... during early childhood. These children do not generally live past age ...
    https://medlineplus.gov/.../infantile-onset-spinocerebellar-ataxia - Genetics