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Results 1 - 10 of 11 for Epilepsy with myoclonic absences
Did you mean Epilepsy with mayoclinic absences?
  1. CHD2 myoclonic encephalopathy 
    ... Some people with CHD2 myoclonic encephalopathy have photosensitive epilepsy, in which seizures are triggered by flashing lights. Some people with CHD2 myoclonic encephalopathy experience a type of seizure called atonic-myoclonic-absence seizure, which begins with a drop of the ...
    https://medlineplus.gov/.../condition/chd2-myoclonic-encephalopathy - Genetics
  2. Childhood absence epilepsy 
    ... muscle rigidity, convulsions, and loss of consciousness, or myoclonic seizures, which are characterized by rapid, uncontrolled muscle jerks. Childhood absence epilepsy affects 2 to 8 in 100,000 children ...
    https://medlineplus.gov/.../condition/childhood-absence-epilepsy - Genetics
  3. SCN8A-related epilepsy with encephalopathy 
    ... begin in infancy.The seizures in SCN8A-related epilepsy with encephalopathy ... (myoclonic seizures), or loss of consciousness with muscle rigidity ...
    https://medlineplus.gov/...cn8a-related-epilepsy-with-encephalopathy - Genetics
  4. Juvenile myoclonic epilepsy 
    ... and loss of consciousness. Sometimes, affected individuals have absence seizures, which cause loss of consciousness for a short period that appears as a staring spell. Typically, people with juvenile myoclonic epilepsy develop the characteristic myoclonic seizures in adolescence, then ...
    https://medlineplus.gov/.../condition/juvenile-myoclonic-epilepsy - Genetics
  5. Spinal muscular atrophy with progressive myoclonic epilepsy 
    ... a variety of seizure types. In addition to myoclonic epilepsy, they may have ... can also have absence seizures, which cause loss of consciousness for a ...
    https://medlineplus.gov/...rophy-with-progressive-myoclonic-epilepsy - Genetics
  6. STXBP1 encephalopathy 
    ... 85 percent of people with STXBP1 encephalopathy develop epilepsy. The most common ... (absence seizures), or loss of consciousness with muscle rigidity ...
    https://medlineplus.gov/genetics/condition/stxbp1-encephalopathy - Genetics
  7. Genetic epilepsy with febrile seizures plus 
    ... called Dravet syndrome (also known as severe myoclonic epilepsy of infancy or ... or absence seizures. In Dravet syndrome, these seizures are difficult ...
    https://medlineplus.gov/...netic-epilepsy-with-febrile-seizures-plus - Genetics
  8. Isolated lissencephaly sequence 
    ... infantile spasms, short periods of loss of consciousness (absence seizures); sudden episodes of weak muscle tone (drop attacks); rapid, uncontrolled muscle jerks (myoclonic seizures); and episodes of muscle rigidity, convulsions, and ...
    https://medlineplus.gov/.../isolated-lissencephaly-sequence - Genetics
  9. Beta-propeller protein-associated neurodegeneration 
    ... have the appearance of staring spells or daydreaming (absence seizures, also called petit mal seizures), sudden episodes of weak muscle tone (atonic seizures), involuntary muscle twitches (myoclonic seizures), or more pronounced movements called epileptic spasms. ...
    https://medlineplus.gov/...ller-protein-associated-neurodegeneration - Genetics
  10. KCNB1 encephalopathy 
    ... characterized by abnormal brain function (encephalopathy), recurrent seizures ... seizures), uncontrolled muscle stiffness (tonic seizures), loss of ...
    https://medlineplus.gov/genetics/condition/kcnb1-encephalopathy - Genetics
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