Turcot's syndrome: evidence for linkage to the adenomatous polyposis coli (APC) locus

Neurology. 1994 Jun;44(6):1083-6. doi: 10.1212/wnl.44.6.1083.

Abstract

Objective: To investigate the possibility that neuroepithelial tumors in Turcot's syndrome are caused by pleiotropic mutations in the gene for adenomatous polyposis coli (APC), a tumor-suppressor gene implicated in colonic cancer.

Methods: We studied the inheritance patterns of genetic markers for the chromosome 5q21 region in 12 members of a Turcot's syndrome kindred with five affected members. We performed linkage analysis to detect linkage between the disease phenotype and DNA markers.

Results: Marker D5S346, located 30 to 70 kilobases from the APC locus, showed evidence highly suggestive of linkage to the disease phenotype (lod score = 1.92).

Conclusions: The data provide evidence that the tumor-suppressor gene implicated in APC and sporadic colon cancers may also cause malignant neuroepithelial tumors in Turcot's syndrome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenomatous Polyposis Coli / genetics*
  • Gardner Syndrome / genetics
  • Genetic Linkage*
  • Genetic Markers
  • Humans
  • Mutation*
  • Neuroectodermal Tumors, Primitive, Peripheral / genetics*
  • Pedigree
  • Syndrome

Substances

  • Genetic Markers