The use of genomic microarrays to study chromosomal abnormalities in mental retardation.

TitleThe use of genomic microarrays to study chromosomal abnormalities in mental retardation.
Publication TypeJournal Article
Year of Publication2005
AuthorsMao R, Pevsner J
JournalMental retardation and developmental disabilities research reviews
Volume11
Issue4
Pagination279-85
Date Published2005
Abstract

Mental retardation affects 2 to 3% of the US population. It is defined by broad criteria, including significantly subaverage intelligence, onset by age 18, and impaired function in a group of adaptive skills. A myriad of genetic and environmental causes have been described, but for approximately half of individuals diagnosed with mental retardation the molecular basis remains unknown. Genomic microarrays, also called array comparative genomic hybridization (array CGH), represent one of several novel technologies that allow the detection of chromosomal abnormalities, such as microdeletions and microduplications, in a rapid, high throughput fashion from genomic DNA samples. In one early application of this technology, genomic microarrays have been used to characterize the extent of chromosomal changes in a group of patients diagnosed with one particular type of disorder that causes mental retardation, such as deletion 1p36 syndrome. In another application, DNA samples from individuals with idiopathic mental retardation have been assayed to scan the entire genome in attempts to identify chromosomal changes. Genomic microarrays offer both a genome-wide perspective of chromosomal aberrations as well as higher resolution (to the level of approximately one megabase) compared to alternative available technologies.

Alternate JournalMent Retard Dev Disabil Res Rev