Blackman J A, Selzer S C, Patil S, Van Dyke D C
Kluge Children's Rehabilitation Center and Research Institute, University of Virginia, Charlottesville 22901.
Dev Med Child Neurol. 1991 Feb;33(2):162-6. doi: 10.1111/j.1469-8749.1991.tb05096.x.
The relationship between a fragile site on the X chromosome and autism has been well documented. The authors report a three-year-old child with partial duplication of the short arm of chromosome Y, who had an autistic disorder. He was microcephalic, but otherwise had a normal phenotype. There was a history of preterm birth and maternal diabetes. This is the sixth case of sex chromosome Y aneuploidy associated with autism, but the first with an isodicentric Y. In well-substantiated cases of autism, clinicians should now consider abnormalities of the Y as well as the X chromosome.