| Literature DB >> 25350348 |
Bryn D Webb1, Rebecca J Scharf, Emily A Spear, Lisa J Edelmann, Annemarie Stroustrup.
Abstract
The goal of molecular cytogenetic testing for children presenting with developmental delay (DD) is to identify or exclude genetic abnormalities that are associated with cognitive, behavioral and/or motor symptoms. Until 2010, chromosome analysis was the standard first-line genetic screening test for evaluation of patients with DD when a specific syndrome was not suspected. In 2010, The American College of Medical Genetics and several other groups recommended chromosomal microarray as the first-line test in children with DDs, multiple congenital anomalies and/or autism. This test is able to detect regions of genomic imbalances at a much finer resolution than G-banded karyotyping. Until recently, no chromosomal microarray testing had been approved by the US FDA. This article focuses on the use of the Affymetrix CytoScan(®) Dx Assay (Santa Clara, CA, USA), the first chromosomal microarray to receive FDA approval for the genetic evaluation of individuals with DD.Entities:
Keywords: Affymetrix CytoScan® Dx Assay; chromosomal microarray; genetic testing; global developmental delay; mental retardation
Mesh:
Year: 2014 PMID: 25350348 PMCID: PMC4415685 DOI: 10.1586/14737159.2015.975213
Source DB: PubMed Journal: Expert Rev Mol Diagn ISSN: 1473-7159 Impact factor: 5.225