| Literature DB >> 12838551 |
Hui-quan Zhao1, Alan F Rope, Howard M Saal, Ruthann I Blough-Pfau, Robert J Hopkin.
Abstract
11q trisomy is associated with a recognizable pattern of multiple malformations. Review of the literature reveals the following recurrent themes common to complex and isolated 11q trisomy: mental retardation, pre- and postnatal growth retardation, hypotonia, a distinct pattern of facial features, congenital heart defects, and limb malformations. We report four patients with partial trisomy 11q, none of which arose from the common 11/22 translocation. Three of the four patients had the previously unreported finding of upper airway obstruction secondary to a malformed epiglottis. The critical region for this malformation appears to be 11q21-23.2. Copyright 2003 Wiley-Liss, Inc.Entities:
Mesh:
Year: 2003 PMID: 12838551 DOI: 10.1002/ajmg.a.20134
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802