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)

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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.