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Results 1 - 10 of 25 for Myoclonic absence seizure
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  1. CHD2 myoclonic encephalopathy 
    ... encephalopathy experience a type of seizure called atonic-myoclonic-absence seizure, which begins with a drop of the head, followed by loss of consciousness, then rigid movements of the arms. Epilepsy ... myoclonic encephalopathy are called refractory because they usually do ...
    https://medlineplus.gov/.../condition/chd2-myoclonic-encephalopathy - Genetics
  2. Genetic epilepsy with febrile seizures plus 
    ... begin in early childhood. These types can include myoclonic or absence seizures. In Dravet syndrome, these seizures are difficult to ...
    https://medlineplus.gov/...netic-epilepsy-with-febrile-seizures-plus - Genetics
  3. Vagus Nerve Stimulator Therapy for Epilepsy (For Parents) (Nemours Foundation)  
    Epilepsy/Children ... Epilepsy ... Nemours Foundation ... Vagus nerve stimulator, epilepsy, epilepsy treatment, vagus, vagal, nerve stimulator, seizures, siezures, seizure, ...
    https://kidshealth.org/en/parents/vagus-nerve-stimulator.html - External Health Links
  4. Absence Seizure (Petit Mal Seizure) (Mayo Foundation for Medical Education and Research)  
    Seizures/Specifics ... Seizures ... Mayo Foundation for Medical Education and Research
    https://www.mayoclinic.org/.../symptoms-causes/syc-20359683?p=1 - External Health Links
  5. SCN8A-related epilepsy with encephalopathy 
    ... infantile spasms), partial or complete loss of consciousness (absence seizures), involuntary muscle twitches (myoclonic seizures), or loss of consciousness with muscle rigidity ...
    https://medlineplus.gov/...cn8a-related-epilepsy-with-encephalopathy - Genetics
  6. EFHC1 gene 
    ... tonic-clonic seizures (or grand mal seizures) and absence seizures. Most gene mutations associated with juvenile myoclonic epilepsy replace single protein building blocks (amino acids) ...
    https://medlineplus.gov/genetics/gene/efhc1 - Genetics
  7. 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 ...
    https://medlineplus.gov/.../condition/childhood-absence-epilepsy - Genetics
  8. Seizures (Nemours Foundation)  
    First Aid/Specifics ... First Aid ... Nemours Foundation ... seizures, seizure, my child is having a seizure, my child had a seizure, sezure, siezure, seisure, siesure, ...
    https://kidshealth.org/en/parents/seizure.html - External Health Links
  9. Epilepsy (Nemours Foundation)  
    Epilepsy/Teenagers ... Epilepsy ... Nemours Foundation ... epilepsy, epilipsy, epelipsy, epylipsy, seizure, seazure, convulsions, electrical signals in the brain, what ...
    https://kidshealth.org/en/teens/epilepsy.html - External Health Links
  10. STXBP1 encephalopathy 
    ... people with this condition include uncontrolled muscle twitches (myoclonic seizures), sudden episodes of weak muscle tone (atonic seizures), partial or complete loss of consciousness (absence seizures), or loss of consciousness with muscle rigidity ...
    https://medlineplus.gov/genetics/condition/stxbp1-encephalopathy - Genetics
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