West Syndrome is a rare and severe form of epilepsy that typically begins in infancy, often between 3 to 12 months of age. It is characterized by a specific type of seizure called infantile spasms, which are sudden, brief contractions of the muscles. These spasms can occur in clusters and may be accompanied by developmental delays. The condition is often associated with underlying issues such as brain injury, genetic disorders, or metabolic problems. Early diagnosis and treatment are crucial, as they can help manage symptoms and improve outcomes for affected children. Treatment options may include medications, dietary changes, or other therapies.