Systematic Screening for Subtelomeric Anomalies in a Clinical Sample of Autism

Authors: Wassink, Thomas¹; Losh, Molly; Piven, Joseph; Sheffield, Val; Ashley, Elizabeth; Westin, Erik; Patil, Shivanand

Source: Journal of Autism and Developmental Disorders, Volume 37, Number 4, April 2007 , pp. 703-708(6)

Publisher: Springer

Key:

- Free Content

- New Content

- Subscribed Content

- Free Trial Content

Abstract:

High-resolution karyotyping detects cytogenetic anomalies in 5-10% of cases of autism. Karyotyping, however, may fail to detect abnormalities of chromosome subtelomeres, which are gene rich regions prone to anomalies. We assessed whether panels of FISH probes targeted for subtelomeres could detect abnormalities beyond those identified by karyotyping in 104 individuals with Pervasive Developmental Disorders (PDDs) drawn from a general clinical population. Four anomalies were detected by karyotyping, while no additional anomalies were detected by subtelomere FISH or by probes targeted for 15q11.2q13 or 22q11.2 in subgroups of our sample. We conclude that while karyotyping may be more broadly indicated for autism than previously supposed, subtelomere FISH appears less likely to be a useful screening tool for unselected PDD populations.

Keywords: Autism; Chromosomal anomalies; FISH; Karyotyping; Subtelomere

Document Type: Research article

DOI: 10.1007/s10803-006-0196-9

Affiliations: 1: Email: thomas-wassink@uiowa.edu

The full text electronic article is available for purchase. You will be able to download the full text electronic article after payment.

$47.00 plus tax Refund Policy