The authors retrospectively identified 17 children with Down syndrome
who developed infantile spasms, and analysed their etiology, EEG findi
ngs, response to medication, development and prognosis. Compared with
symptomatic infantile spasms in the general population, which have a p
oor prognosis, these patients had a relatively benign outcome with reg
ard to seizure control: only three of 16 survivors currently have seiz
ures and seven of the 16 currently receive anticonvulsants. Developmen
tal outcome was poorest in those with a superimposed hypoxic insult an
d in those who regressed developmentally at the onset of the spasms an
d did not regain developmental milestones. The overall neurological pr
ognosis for children with Down syndrome and infantile spasms appears t
o be better than for children with infantile spasms in the general pop
ulation.