Deletion 10q23.2-q23.33 in a patient with gastrointestinal juvenile polyposis and other features of a Cowden-like syndrome

Genes Chromosomes Cancer. 1998 Feb;21(2):113-8. doi: 10.1002/(sici)1098-2264(199802)21:2<113::aid-gcc6>;2-3.


A cytogenetically visible interstitial deletion of chromosome band 10q23 was found in a 6-year-old boy with mental retardation, dysmorphic features, and juvenile polyposis coli. In order to map this patient's deletion physically, we performed fluorescence in situ hybridization by using yeast artificial chromosomes (YACs) in the vicinity of the deletion. Five YACs that span an 11-15 cM region within the deletion were identified. This patient's deletion contains the putative locus for Cowden syndrome and a recently discovered candidate tumor suppressor gene (MMAC1 or PTEN) that has been implicated in the progression of a variety of human malignancies. Furthermore, the deletion is near and possibly overlaps a locus associated with juvenile polyposis. The findings in this patient with a constitutional 10q23 deletion raise the issue of whether there are separate genes in this region that are involved in Cowden syndrome, Bannayan-Riley-Ruvalcaba syndrome, juvenile polyposis, and tumor progression, or whether all of these entities could be due to a single gene.

Publication types

  • Case Reports

MeSH terms

  • Child
  • Chromosome Deletion*
  • Chromosomes, Artificial, Yeast
  • Chromosomes, Human, Pair 10 / genetics*
  • Genes, Tumor Suppressor / genetics
  • Germ-Line Mutation / genetics
  • Hamartoma Syndrome, Multiple / genetics*
  • Humans
  • In Situ Hybridization, Fluorescence
  • Intestinal Polyps / genetics*
  • Karyotyping
  • Male