Congenital (congenital) myasthenic syndrome caused by a compound-heterozygous mutation in the CHAT gene, involving the muscles of the extremities

purchase of Firdaps for 6 months

Focal cortical dysplasia (Lenox-Gastaut symptom complex)

examination and surgical treatment at the Bethel Epilepsy Center at the Mara Clinic (Germany)

bilateral atresia of the external auditory canal, microtia of the external ear on the left

operation to form the external auditory canal on the right (the first stage of hearing restoration) at the International Center for the Treatment of Atresia and Microtia (California, USA)

structural localized epilepsy

check-up and treatment in the German clinic (Epilepsy Centre Bethel)

congenital abnormalities (ear), microtia and atresia (external ear canal), dextral dull of hearing

external ear reconstruction

short bowel syndrome (SBS)

Infusomat B Braun Space + expendable materials,
nutritional support (six-month course)

congenital Eaton-Lambert syndrome secondary to heterozygous mutation in CHAT gene

acquisition of medicament Firdapse