“There is growing evidence that many autistic people have related genetic defects, or defects that are exacerbated by this one,” said Yu Yamaguchi, M.D., Ph.D., professor in the Sanford Children’s Health Research Center at Sanford-Burnham. Children with
Research on Rare Bone Disorder Reveals New Insights into Autism
2012-03-13T17:15:51-04:00By Ollibean|Categories: Articles, General, Medical|Tags: ASD, autism, Autism Spectrum Disorders, heparan sulfate, MHE, multiple hereditary exostoses, rare or undiagnosed disorders|0 Comments
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Ollibean is a dynamic community of parents, families and advocates in the disability community working together for a more socially just, accessible and inclusive world.
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