Gardner syndrome in a boy with interstitial deletion of the long arm of chromosome 5

Am J Med Genet. 1991 Dec 15;41(4):460-3. doi: 10.1002/ajmg.1320410416.

Abstract

We described a 15-year-old boy with Gardner syndrome (GS), mental retardation, and craniofacial abnormalities. High-resolution banding analysis showed an interstitial deletion of the long arm of chromosome 5 (q22.1----q31.1). The breakpoints in the present case and in 3 previously reported 5q- patients with adenomatous polyposis coli suggest that the gene responsible for GS/or familial polyposis coli (FPC) is in the 5q22 region, a result consistent with the findings of linkage studies.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Abnormalities, Multiple / genetics
  • Adolescent
  • Chromosome Banding
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 5*
  • Gardner Syndrome / genetics*
  • Humans
  • Intellectual Disability / genetics
  • Male