June 1988

Association of Autism, Retinoblastoma, and Reduced Esterase D Activity

Author Affiliations

Division of Mental Retardation and Child Psychiatry
Departments of Neurology and Pediatrics
Department of Medicine UCLA School of Medicine Los Angeles, CA 90024

Arch Gen Psychiatry. 1988;45(6):600. doi:10.1001/archpsyc.1988.01800300098019

To the Editor.—  We wish to report the simultaneous occurrence of autism, sporadic retinoblastoma, reduced esterase D activity, and a deletion on chromosome 13 in a 19-year-old woman with an autistic maternal second cousin.The patient was born following an apparently normal pregnancy and delivery. She was identified as developmentally delayed by the end of her first year of life. At age 2Vz years, a retinoblastoma of the right eye was removed by enucleation. No radiation was given, and her left eye remained uninvolved. The diagnosis of autism was established by repeated developmental, psychiatric, psychologic, and educational assessments (DSM-III1 and National Society for Autistic Children2 criteria). Mental status examination by one of us (E.R.R.) confirmed the diagnosis of autism, full syndrome present (DSM-III 299.0).1 The red blood cell esterase D level was 50% normal, and trypsin-Giemsa chromosome banding analysis revealed a deletion on the long arm of

First Page Preview View Large
First page PDF preview
First page PDF preview