“May all be happy, may all be healed, may all be at peace and may no one ever suffer."
Infantile spasms, also known as West syndrome, is a rare form of epilepsy that typically begins in infants between the ages of 3 and 12 months. The condition is characterized by sudden and frequent muscle spasms, often occurring in clusters, and may be accompanied by other symptoms such as developmental delays, intellectual disability, and behavioral problems.
The exact cause of infantile spasms is not known, but it is believed to be related to underlying brain abnormalities or genetic mutations. In some cases, the condition may be associated with other neurological or genetic disorders.
Treatment for infantile spasms typically involves medications to control seizures, such as adrenocorticotropic hormone (ACTH) or corticosteroids, which may be administered orally or through injections. Other medications may also be used as adjunct therapy, depending on the underlying cause of the condition. In some cases, surgery or other interventions may be necessary to manage the condition or underlying disorders.
It is important to seek medical attention promptly if you suspect your infant may be experiencing symptoms of infantile spasms or any other seizure disorder. Early diagnosis and treatment can help to improve outcomes and quality of life for affected individuals.