A previously undescribed de novo 4p15 deletion in a patient with apparently isolated metopic craniosynostosis

Am J Med Genet A. 2011 Oct;155A(10):2543-51. doi: 10.1002/ajmg.a.34201. Epub 2011 Sep 9.

Abstract

Interstitial deletion of the short arm of chromosome 4, excluding cytoband p16, has been described as a distinct phenotype from the Wolf-Hirschhorn syndrome, characterized by a deletion encompassing cytoband p16. We report on the case of a 14-month-old boy with an apparently isolated craniosynostosis and harboring a de novo microdeletion in band 4p15. The imbalance, about 4 Mb in size is, to date, the smallest deletion ever described in this region, encompassing 12 genes. A comparison with other previously described cases of 4p15 deletion is made, and the possible roles of some genes involved in the deletion are discussed.

Publication types

  • Case Reports

MeSH terms

  • Chromosome Deletion
  • Chromosomes, Human, Pair 4 / genetics
  • Comparative Genomic Hybridization
  • Craniosynostoses / genetics*
  • Craniosynostoses / pathology*
  • Humans
  • In Situ Hybridization, Fluorescence
  • Infant
  • Karyotyping
  • Male

Supplementary concepts

  • Chromosome 4 short arm deletion