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Results 1 - 10 of 11 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. 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
  3. 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
  4. 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
  5. 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
  6. 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
  7. Isolated lissencephaly sequence 
    ... be severe enough to cause brain dysfunction (epileptic encephalopathy). After ... (myoclonic seizures); and episodes of muscle rigidity, convulsions, and ...
    https://medlineplus.gov/.../isolated-lissencephaly-sequence - Genetics
  8. Genetic epilepsy with febrile seizures plus 
    ... types of seizure in people with GEFS+ include myoclonic seizures, which cause involuntary muscle twitches; atonic seizures, ... condition called Dravet syndrome (also known as severe myoclonic epilepsy of infancy or SMEI) is often considered ...
    https://medlineplus.gov/...netic-epilepsy-with-febrile-seizures-plus - Genetics
  9. Asparagine synthetase deficiency 
    ... rigidity, and convulsions (tonic-clonic); involuntary muscle twitches (myoclonic); or abnormal muscle contraction (tonic). People with asparagine ... the condition. ASNS deficiency ASNSD Congenital microcephaly-severe encephalopathy-progressive cerebral atrophy syndrome Disorder of asparagine metabolism ...
    https://medlineplus.gov/.../asparagine-synthetase-deficiency - Genetics
  10. Beta-propeller protein-associated neurodegeneration 
    ... weak muscle tone (atonic seizures), involuntary muscle twitches (myoclonic seizures), or more pronounced movements called epileptic spasms. ... Neurodegeneration with brain iron accumulation 5 SENDA Static encephalopathy of childhood with neurodegeneration in adulthood Genetic Testing ...
    https://medlineplus.gov/...ller-protein-associated-neurodegeneration - Genetics
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