Literature DB >> 12838551

Upper airway malformation associated with partial trisomy 11q.

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.

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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


  6 in total

1.  Congenital diaphragmatic hernia associated with duplication of 11q23-qter.

Authors:  M Klaassens; D A Scott; M van Dooren; R Hochstenbach; H J Eussen; W W Cai; R J Galjaard; C Wouters; M Poot; J Laudy; B Lee; D Tibboel; A de Klein
Journal:  Am J Med Genet A       Date:  2006-07-15       Impact factor: 2.802

2.  Phenotypic delineation of Emanuel syndrome (supernumerary derivative 22 syndrome): Clinical features of 63 individuals.

Authors:  Melissa T Carter; Stephanie A St Pierre; Elaine H Zackai; Beverly S Emanuel; Kym M Boycott
Journal:  Am J Med Genet A       Date:  2009-08       Impact factor: 2.802

3.  A 54 Mb 11qter duplication and 0.9 Mb 1q44 deletion in a child with laryngomalacia and agenesis of corpus callosum.

Authors:  Meena Lall; Seema Thakur; Ratna Puri; Ishwar Verma; Mithali Mukerji; Pankaj Jha
Journal:  Mol Cytogenet       Date:  2011-09-21       Impact factor: 2.009

Review 4.  Molecular cytogenetic characterization of partial trisomy of the long arm of chromosome 11 in a patient with multiple congenital anomalies.

Authors:  Austin Walker; Xianfu Wang; Young Mi Kim; Xianglan Lu; Ashley Taylor; Danielle Demarzo; Shibo Li; Hui Pang
Journal:  Mol Cytogenet       Date:  2022-04-19       Impact factor: 1.904

5.  Clinical and molecular evaluations of siblings with "pure" 11q23.3-qter trisomy or reciprocal monosomy due to a familial translocation t (10;11) (q26;q23.3).

Authors:  Rongyu Chen; Chuan Li; Bobo Xie; Jin Wang; Xin Fan; Jingsi Luo; Xuyun Hu; Shaoke Chen; Yiping Shen
Journal:  Mol Cytogenet       Date:  2014-12-24       Impact factor: 2.009

6.  Newborn with Supernumerary Marker Chromosome Derived from Chromosomes 11 And 22- A Case Report.

Authors:  Mohammad Yahya Vahidi Mehrjardi; Masoud Dehghan Tezerjani; Mahmoud Nori-Shadkam; Seyed Mehdi Kalantar; Mohammadreza Dehghani
Journal:  Iran J Public Health       Date:  2016-03       Impact factor: 1.429

  6 in total

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