The condition, traditionally seen as genetic and originating in the brain, is starting to be viewed in a broader and very different light, as a possible immune and neuroinflammatory disorder. As a result, autism is beginning to look like a condition that can, in some and perhaps many cases, be successfully treated.Of course, the idea of autism as a treatable disorder is very exciting. But (of course!) it's not that easy.
Neimark joins a growing stream of writers and researchers who feel that there is not just one "autism" but rather many "autisms." These different "autisms" probably include different sets of symptoms ranging from apraxia to sleep issues to gastrointestinal problems to sensory processing challenges. Your child could be a "non-verbal sensory craver with a touch of diarrhea," while the boy down the street is a "hyperlexic sleep-deprived savant!"
So - how will researchers and clinicians decide to sort our children? How will they evaluate and diagnose? Will the same treatments work for all of the children in any given group? This - and so much more - is still very much up for grabs!

From my research and experience some or a great of sporadic autism is primarily genetic and due to advanced paternal age with its increasing spontaneous mutations. Environmental toxins such as PERC can damage sperm DNA as well as excessive coffee drinking. Anything that can mutate the genes of the spermatagonia, ancestral sperm making cells and sperm can be enough to cause autism as the mutations accumulate with the number of cell divisons per year of age. Advancing paternal age is the number 1 suspect for me on a population level, and would include the effects of toxins affecting sperm DNA. Some men start out with genes that are already unstable due to advanced paternal age etc. in prior generations. Fathering babies up to about age 33 and cryo-preserving semen in ones mid 20s or very early early 30s would decrease the incidence of non-familial autism.
http://themalebiologicalclock.blogspot.com/