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ScienceDaily (June 23, 2008) — UCLA researchers discovered that an FDA-approved drug reverses the brain dysfunction inflicted by a genetic disease called tuberous sclerosis complex (TSC). Because half of TSC patients also suffer from autism, the findings offer new hope for addressing learning disorders due to autism. Nature Medicine publishes the findings in its online June 22 edition.
"After only three days of treatment, the TSC mice learned as quickly as the healthy mice," said Ehninger. "The rapamycin corrected the biochemistry, reversed the learning deficits and restored normal hippocampal function, allowing the mice's brains to store memories properly."
Originally posted by Long Lance
good news if the results are permanent.
"After only three days of treatment, the TSC mice learned as quickly as the healthy mice," said Ehninger. "The rapamycin corrected the biochemistry, reversed the learning deficits and restored normal hippocampal function, allowing the mice's brains to store memories properly."
strangely, a single period of treatment seems to cure the affliction, which sounds much more like a deficiency disease, doesn't it? how could a genetic aberration be remedied without continuous application?
Originally posted by Long Lance
reply to post by sir_chancealot
no catalyst/enzyme lasts forever, ...