Angelina Shpeneva

   Little Angelina's epilepsy debuted at the age of 4.5 months. It has a pharmacoresistant course. As of now, the girl has experienced numerous epileptic seizures every day. The genetic component of the disease is not excluded by doctors. The presence of a pathogenic mutation will affect the choice of treatment strategies. Epilepsy occurs in the form of epileptic encephalopathy of Lennox-Gastaut syndrome with the presence of daily tonic, myoclonic seizures and atypical absences. The child needs to conduct a genetic study - the panel "hereditary epilepsies". Angelina was supported by «Chance» program.