
The first study involved abnormalities related to a chromosomal region in the brain, the deletion of which causes Phelan-McDermind syndrome, a disorder characterized by developmental delay and language impairments. The set of genes are also related to autism. Researchers analyzed brain images of ten individuals who had the particular genes deleted. Eight of the group had a smaller-than-normal vermis, which connects the halves of the cerebellum, and an enlarged cavity for the cerebellum. These abnormalities have also been observed in people with autism.
Another study assessed over 3,000 mouse genes, finding two ‘cliques’ of genes, many of which may be related to autism. Both of these gene groups were located in the cerebellum. The researchers had anticipated that the majority of autism candidate genes would be in the cerebral cortex, rather than the cerebellum.
A third study noted the relationship between Purkinje cells (long, branching neurons found in the cerebellum) and autistic brains. Brains of people with ASD have fewer Purkinje cells than normal. Additional research demonstrated that mice lacking a particular gene that causes Purkinje degeneration exhibit autism-like behavior.
Finally, another mice-based study focused on how dopamine is released when the brain lacks Purkinje cells. The researchers studied dopamine pathways in mice that had lost all of their Purkinje cells. The mice’s brains were stimulated to cause a release of dopamine. The mice without Purkinje cells had a lower dopamine release in the prefrontal cortex than the controls.
Some researchers are developing the idea that the cerebellum may be at the root of autism. “Cerebellar dysfunction may be contributing to impaired coordination of social actions in parallel to the ways it contributes to impaired coordination of motor actions,” stated Stewart Mostofsky, director of the Laboratory for Neurocognitive and Imaging Research at Baltimore’s Kennedy Krieger Institute.
This literature review is available via SFARI.org.
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