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Results 1 - 10 of 17 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. 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
  4. 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
  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. 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
  8. 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
  9. 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
  10. CSTB gene 
    ... to cause the signs and symptoms of progressive myoclonic epilepsy type 1, but ... and encephalopathy (abnormal brain function). These symptoms resemble those seen ...
    https://medlineplus.gov/genetics/gene/cstb - Genetics
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