7p22.2 Microduplication: A Pathogenic CNV?

Genes (Basel). 2023 Jun 19;14(6):1292. doi: 10.3390/genes14061292.

Abstract

Partial duplication of the short arm of chromosome 7 is a rare chromosome rearrangement. The phenotype spectrum associated with this rearrangement is extremely variable even if in the last decade the use of high-resolution microarray technology for the investigation of patients carrying this rearrangement allowed for the identification of the 7p22.1 sub-band causative of this phenotype and to recognize the corresponding 7p22.1 microduplication syndrome. We report two unrelated patients that carry a microduplication involving the 7.22.2 sub-band. Unlike 7p22.1 microduplication carriers, both patients only show a neurodevelopmental disorder without malformations. We better characterized the clinical pictures of these two patients providing insight into the clinical phenotype associated with the microduplication of the 7p22.2 sub-band and support for a possible role of this sub-band in the 7p22 microduplication syndrome.

Keywords: 7p22; 7p22.2 microduplication; CNV; SDK11; array-CGH. 7p22.1; minimal critical region; neurodevelopmental phenotypes.

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple* / genetics
  • Chromosome Duplication
  • Chromosome Structures
  • Humans
  • Intellectual Disability* / genetics
  • Trisomy

Grants and funding

This research received no external funding.