Information on Infantile Spasms

Infantile spasms also called West syndrome. InfantileThe standard pattern of infantile spasms features
spasms are an uncommon to rare and grave form ofminor head bobbing. Eventually, the child starts to have
epilepsy in infants. About 60% of the affected infantsflexor, extensor, or mixed spasms. Flexor spasms are
have some brain disorder or brain injury before thethe most common. The child’s neck, arms, and legs
seizures begin, but the others have had no apparentdraw towards his chest. The child frequently bends at
injury and have been developing normally. Infantilethe waist in a “jackknife” motion. Extensor
spasm (IS) is a specific type of seizure seen in anspasms are the least common. The child’s neck,
epilepsy syndrome of infancy. The syndrome isarms, and legs stretch out. Mixed spasms, in which the
age-related, generally occurring between the third andchild’s arms and body contract and his legs stretch
the twelfth month, generally manifesting around theout, are also very common. The goals of treatment for
fifth month. The syndrome is often caused by aninfants with West syndrome are the best quality of life
organic brain dysfunction whose origins may bewith no seizures, the fewest adverse effects from
prenatal, perinatal or postnatal.treatment, and the least number of medications.
Eighty-five percent of kids who increase infantileSteroid therapy is the first treatment for infantile
spasms do so before the age of twelve months; mostspasms. Antiepileptic medications, such as vigabatrin
end having spasms by age 5. During this period, 40(currently not approved for use in the US) have shown
percent will have other types of seizures. It is likely thatsome efficacy. Sabril is often used as the initial therapy
one child in every 2,200 to 4,500 children born will growbecause it is relatively secure and helpful. It is especially
infantile spasms. More boys than girls develop infantileeffective for children with tuberous sclerosis (a
spasms, but the figures vary. Bio-chemical mechanismsdisorder associated with abnormalities involving the
lead to the occurrence of West syndrome. It isbrain, skin, heart, and other parts of the body). If the
conjectured that it is a malfunction of theseizures are caused by a focal brain abnormality such
neurotransmitter function, or more precisely, aas a tumour or a cyst, surgery to remove the
malfunction in the regulation of the GABA transmissionabnormality. The ketogenic diet has been employed
process.successfully to treat a variety of seizure types.