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Results 11 - 20 of 20 for Infantile encephalopathy
  1. Epilepsy of infancy with migrating focal seizures 
    ... DEE 14 Developmental and epileptic encephalopathy 14 Early infantile epileptic encephalopathy 14 EIEE14 EIMFS Epilepsy with migrating focal seizure ...
    https://medlineplus.gov/...-of-infancy-with-migrating-focal-seizures - Genetics
  2. GRIN2B-related neurodevelopmental disorder 
    ... disorder in their family. EIEE27 Epileptic encephalopathy, early infantile, 27 GRIN2B encephalopathy GRIN2B related syndrome Genetic Testing Registry: Developmental and ...
    https://medlineplus.gov/...rin2b-related-neurodevelopmental-disorder - Genetics
  3. Leigh syndrome 
    ... there is no family history of this condition. Infantile subacute necrotizing encephalopathy Juvenile subacute necrotizing encephalopathy Leigh disease Leigh's ...
    https://medlineplus.gov/genetics/condition/leigh-syndrome - Genetics
  4. Isolated lissencephaly sequence 
    ... with ILS have a type of seizure called infantile spasms, these seizures can be severe enough to cause brain dysfunction (epileptic encephalopathy). After the first months of life, most children ...
    https://medlineplus.gov/.../isolated-lissencephaly-sequence - Genetics
  5. MEGDEL syndrome 
    ... Manov I, Saada A, Sprecher E, Mandel H. Infantile mitochondrial hepatopathy is a cardinal feature of MEGDEL syndrome (3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome) caused by novel mutations ...
    https://medlineplus.gov/genetics/condition/megdel-syndrome - Genetics
  6. Infantile-onset spinocerebellar ataxia 
    ... 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 Citation on PubMed Lonnqvist T. Infantile-Onset Spinocerebellar Ataxia - RETIRED CHAPTER, FOR HISTORICAL REFERENCE ...
    https://medlineplus.gov/.../infantile-onset-spinocerebellar-ataxia - Genetics
  7. Lennox-Gastaut syndrome 
    ... 2014 Sep 29. Citation on PubMed Trevathan E. Infantile spasms ... genes in epileptic encephalopathies. Genes Brain Behav. 2018 Nov;17(8):e12456. ...
    https://medlineplus.gov/genetics/condition/lennox-gastaut-syndrome - Genetics
  8. Combined oxidative phosphorylation deficiency 1 
    ... Norsiah MD, van den Heuvel LP, Rodenburg RJ. Infantile Progressive Hepatoencephalomyopathy with Combined OXPHOS Deficiency due to ... Long-term survival in a child with severe encephalopathy, multiple respiratory chain deficiency and GFM1 mutations. Front ...
    https://medlineplus.gov/...ed-oxidative-phosphorylation-deficiency-1 - Genetics
  9. Ornithine translocase deficiency 
    ... translocase deficiency are usually less severe than the infantile form.Infants with ornithine translocase deficiency may lack ... coordination (ataxia), vision problems, episodes of brain dysfunction (encephalopathy), developmental delay, learning disabilities, or stiffness caused by ...
    https://medlineplus.gov/.../ornithine-translocase-deficiency - Genetics
  10. GLUT1 deficiency syndrome 
    ... DC. Brain glucose supply and the syndrome of infantile neuroglycopenia. Arch Neurol. 2007 Apr;64(4):507- ...
    https://medlineplus.gov/genetics/condition/glut1-deficiency-syndrome - Genetics
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