Drug of choice for infantile spasm is –

Myoclonic epilepsy may be Infantile spasm or Infantile myoclonus or West syndrome Juvenile myoclonic epilepsy Infantile spasm (Infantile mvoclonus or west syndrome) The onset is usually between 3-8 months of life It is characterized by a triad of - i) Salaam spells (sudden dropping of the head & flexion of arms) ii) Mental retardation iii) Hypsarrhythmic pattern of EEG (diffuse high voltage slow spike and chaotic activity) The spasm occurs in clusters usually on waking. Prognosis for normal mental development is poor. Treatment of infantile myoclonus ACTH and corticosteroids are given for 2-12 weeks, depending upon response. Vigabatrin is the DOC Now.