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Results 1 - 10 of 23 for Myoclonic encephalopathy
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  1. CHD2 myoclonic encephalopathy 
    CHD2 myoclonic encephalopathy is a condition characterized by recurrent seizures (epilepsy), abnormal brain function (encephalopathy), and intellectual disability. Epilepsy begins ...
    https://medlineplus.gov/.../condition/chd2-myoclonic-encephalopathy - Genetics
  2. CHD2 gene 
    ... CHD2 gene have been found to cause CHD2 myoclonic encephalopathy, a condition characterized by recurrent seizures (epilepsy), abnormal ... lead to the signs and symptoms of CHD2 myoclonic encephalopathy. More About This Health Condition At least nine ...
    https://medlineplus.gov/genetics/gene/chd2 - Genetics
  3. Epilepsy (National Library of Medicine)  
    Epilepsy is a brain disorder that causes people to have recurring seizures. The seizures happen when clusters of nerve cells, or neurons, in the brain send out ...
    https://medlineplus.gov/epilepsy.html - Health Topics
  4. 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
  5. SCN8A-related epilepsy with encephalopathy 
    ... loss of consciousness (absence seizures), involuntary muscle twitches (myoclonic seizures), or loss of consciousness with muscle rigidity and convulsions (tonic-clonic seizures). Most people with SCN8A-related epilepsy with encephalopathy have more than one type of seizure. The ...
    https://medlineplus.gov/...cn8a-related-epilepsy-with-encephalopathy - Genetics
  6. ARX gene 
    ... 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
  7. Lennox-Gastaut syndrome 
    Lennox-Gastaut syndrome is a severe condition characterized by repeated seizures (epilepsy) that begin early in life. Affected individuals have multiple types ...
    https://medlineplus.gov/genetics/condition/lennox-gastaut-syndrome - Genetics
  8. STXBP1 encephalopathy 
    ... people with this condition include uncontrolled muscle twitches (myoclonic ... who have STXBP1 encephalopathy have more than one type of seizure. In ...
    https://medlineplus.gov/genetics/condition/stxbp1-encephalopathy - Genetics
  9. KCNB1 encephalopathy 
    ... people with this condition include uncontrolled muscle twitches (myoclonic ... with KCNB1 encephalopathy do not develop seizures, but they do have ...
    https://medlineplus.gov/genetics/condition/kcnb1-encephalopathy - Genetics
  10. POLG gene 
    ... Condition MedlinePlus Genetics provides information about Mitochondrial neurogastrointestinal encephalopathy disease More About This Health Condition Variants in the POLG gene cause another POLG-related disorder called myoclonic epilepsy myopathy sensory ataxia (MEMSA), which is characterized ...
    https://medlineplus.gov/genetics/gene/polg - Genetics
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