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https://www.ncbi.nlm.nih.gov/books/NBK619245/
KCTD7-Related Progressive Myoclonic Epilepsy - GeneReviews® - NCBI Bookshelf
KCTD7-related progressive myoclonic epilepsy (KCTD7-PME) is characterized by early-onset myoclonic seizures that are frequently pharmacoresistant and...
ncbi bookshelfrelatedprogressivemyoclonicepilepsy
https://epilepsyfoundation.org.au/understanding-epilepsy/epilepsy-syndromes/juvenile-myoclonic-epilepsy-jme/
Juvenile Myoclonic Epilepsy (JME) | Epilepsy Foundation
JME is a fairly common epilepsy syndrome that usually begins between the ages of 12 to 18 years. Seizure symptoms include myoclonic jerking of the shoulders…
juvenilemyoclonicepilepsyjmefoundation
https://epilepsyfoundation.org.au/understanding-epilepsy/epilepsy-syndromes/early-myoclonic-encephalopathy-eme/
Early Myoclonic Encephalopathy (EME) | Epilepsy Foundation
EME is a rare epilepsy syndrome which is usually diagnosed before 3 months of age, and often the first seizure could be felt in the womb of a mother during…
epilepsy foundationearlymyoclonicencephalopathyeme
https://epilepsyfoundation.org.au/understanding-epilepsy/epilepsy-syndromes/epilepsy-with-myoclonic-atonic-seizures-emas/
Epilepsy with Myoclonic Atonic Seizures (EMAS) | Epilepsy Foundation
Epilepsy with myoclonic-atonic seizures (EMAS) was formerly known as myoclonic-astatic epilepsy (MAE) or Doose Syndrome. It is an uncommon childhood epilepsy…
epilepsymyoclonicseizuresemasfoundation