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Results 1 - 10 of 16 for Early myoclonic encephalopathy
Did you mean Early mayoclinic encephalopathy?
  1. ARX gene 
    ... syndromes, including X-linked lissencephaly with abnormal genitalia, early infantile epileptic encephalopathy 1, and Partington syndrome (described above). Another is X-linked myoclonic epilepsy with intellectual disability and spasticity, which causes ...
    https://medlineplus.gov/genetics/gene/arx - Genetics
  2. CHD2 myoclonic encephalopathy 
    ... lead to the signs and symptoms of CHD2 myoclonic encephalopathy. ... of reproductive cells (eggs or sperm) or in early embryonic development. These cases occur in people with ...
    https://medlineplus.gov/.../condition/chd2-myoclonic-encephalopathy - Genetics
  3. KCNB1 encephalopathy 
    ... family. Early infantile epileptic encephalopathy 26 EIEE26 Epileptic encephalopathy, early infantile, 26 KCNB1-related epilepsy Genetic Testing Registry: ...
    https://medlineplus.gov/genetics/condition/kcnb1-encephalopathy - Genetics
  4. STXBP1 encephalopathy 
    ... STXBP1-related developmental and epileptic encephalopathy STXBP1-related early-onset encephalopathy STXBP1-related epileptic encephalopathy Genetic Testing Registry: Developmental ...
    https://medlineplus.gov/genetics/condition/stxbp1-encephalopathy - Genetics
  5. 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
  6. TBC1D24 gene 
    ... been identified in people with a form of early-infantile epileptic encephalopathy (EIEE16; also called malignant migrating partial seizures of ...
    https://medlineplus.gov/genetics/gene/tbc1d24 - Genetics
  7. Familial encephalopathy with neuroserpin inclusion bodies 
    Familial encephalopathy with neuroserpin inclusion bodies (FENIB) is a disorder that causes progressive dysfunction of the brain (encephalopathy). It is characterized ...
    https://medlineplus.gov/...lopathy-with-neuroserpin-inclusion-bodies - Genetics
  8. Genetic epilepsy with febrile seizures plus 
    ... Other seizure types, including afebrile seizures, begin in early childhood. These types can include myoclonic or absence seizures. In Dravet syndrome, these seizures ...
    https://medlineplus.gov/...netic-epilepsy-with-febrile-seizures-plus - Genetics
  9. Landau-Kleffner Syndrome From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Aphasia/Children ... Aphasia ... Genetic and Rare Diseases Information Center ... From the National Institutes of Health ... Find symptoms and other information about Landau- ...
    https://rarediseases.info.nih.gov/.../6855/landau-kleffner-syndrome - External Health Links
  10. 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
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