Mosaic FMR1 Deletion Causes Fragile X Syndrome and Can Lead to Molecular Misdiagnosis

• Type of Material: Article
• Authors: Brad Coffee, Emory University; Morna Ikeda, Emory University; Dejan B. Budimirovic, Johns Hopkins University; Lawrence N. Hjelm, Emory University; Walter E. Kaufmann, Johns Hopkins University; Stephen Warren, Emory University
• Language: English
• Date: 2008-05-15
• Publisher: Wiley: 12 months
• Publication Version: Author Accepted Manuscript (After Peer Review)
• Copyright Statement: © 2008 Wiley-Liss, Inc.
• Final Published Version (URL): http://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.32261/abstract
• Title of Journal or Parent Work: American Journal of Medical Genetics Part A
• ISSN: 1552-4825
• Volume: 146A
• Issue: 10
• Start Page: 1358
• End Page: 1367
• Grant/Funding Information: This work was supported, in part, by NIH grants HD020521 and HD24064 to STW.
• Keywords: deletion; fragile X syndrome; mosaic; social anxiety; mental retardation
• Research Categories: Biology, Genetics

Abstract

The most common cause of fragile X syndrome is expansion of a CGG trinucleotide repeat in the 5′UTR of FMR1. This expansion leads to transcriptional silencing of the gene. However, other mutational mechanisms, such as deletions of FMR1, also cause fragile X syndrome. The result is the same for both the expansion mediated silencing and deletion, absence of the gene product, FMRP. We report here on an 11-year-old boy with a cognitive and behavioral profile with features compatible with, but not specific to, fragile X syndrome. A mosaic deletion of 1,013,395 bp was found using high-density X chromosome microarray analysis followed by sequencing of the deletion breakpoints. We review the literature of FMR1 deletions and present this case in the context of other FMR1 deletions having mental retardation that may or may not have the classic fragile X phenotype.