J Pediatr Genet 2015; 04(01): 034-037
DOI: 10.1055/s-0035-1554980
Case Report
Georg Thieme Verlag KG Stuttgart · New York

A Case of the 7p22.2 Microduplication: Refinement of the Critical Chromosome Region for 7p22 Duplication Syndrome

Devin M. Cox
1   Department of Psychiatry, University of Kansas Medical Center, Kansas City, Kansas, United States
2   Department of Behavioral Sciences and Pediatrics, University of Kansas Medical Center, Kansas City, Kansas, United States
,
Merlin G. Butler
1   Department of Psychiatry, University of Kansas Medical Center, Kansas City, Kansas, United States
2   Department of Behavioral Sciences and Pediatrics, University of Kansas Medical Center, Kansas City, Kansas, United States
› Author Affiliations
Further Information

Publication History

11 December 2014

01 March 2015

Publication Date:
17 July 2015 (online)

Abstract

We report a 14-year-old Hispanic male with a microduplication of the chromosome 7p22.2 band detected through microarray analysis. He had a history of developmental delay and mild intellectual disability, asthma, myopia, proportionate short stature, dysmorphic features, and Achilles tendon release. This appears to be the first report of a patient with a microduplication of only the chromosome 7p22.2 band and is now the smallest reported duplication to date to include features in common with the chromosome 7p22 duplication syndrome.

 
  • References

  • 1 Chui JV, Weisfeld-Adams JD, Tepperberg J, Mehta L. Clinical and molecular characterization of chromosome 7p22.1 microduplication detected by array CGH. Am J Med Genet A 2011; 155A (10) 2508-2511
  • 2 Papadopoulou E, Sifakis S, Sarri C , et al. A report of pure 7p duplication syndrome and review of the literature. Am J Med Genet A 2006; 140 (24) 2802-2806
  • 3 Preiksaitiene E, Kasnauskiene J, Ciuladaite Z, Tumiene B, Patsalis PC, Kučinskas V. Clinical and molecular characterization of a second case of 7p22.1 microduplication. Am J Med Genet A 2012; 158A (5) 1200-1203
  • 4 Vulto-van Silfhout AT, de Brouwer AF, de Leeuw N, Obihara CC, Brunner HG, de Vries BB. A 380-kb duplication in 7p22.3 encompassing the LFNG gene in a boy with Asperger syndrome. Mol Syndromol 2012; 2 (6) 245-250
  • 5 Firth HV, Richards SM, Bevan AP , et al. DECIPHER: database of chromosomal imbalance and phenotype in humans using Ensembl resources. Am J Hum Genet 2009; 84 (4) 524-533
  • 6 Yamagata M, Weiner JA, Sanes JR. Sidekicks: synaptic adhesion molecules that promote lamina-specific connectivity in the retina. Cell 2002; 110 (5) 649-660