Turcot syndrome

From Wikipedia, the free encyclopedia

You have new messages (last change).

Turcot syndrome is the association between familial adenomatous polyposis and brain tumors like medulloblastoma,malignant glioma. It was first reported by Canadian surgeon Jacques Turcot (1914- ) et al in 1959 and hence carries the first author's name.[1]

The genetic basis of Turcot syndrome is uncertain.The gene most likely to be involved is APC gene in chromosome 5q.[2] However, the syndrome has been claimed to be linked to various mutations in a number of genes. For example, the mismatch repair genes MLH1 (Mendelian Inheritance in Man (OMIM) 120436) or PMS2 (Mendelian Inheritance in Man (OMIM) 600259).

[edit] Synonyms

  • Brain tumor-polyposis syndrome
  • Glioma-polyposis syndrome

[edit] External link

[edit] Reference

  1. ^ Turcot J, Després JP, St. Pierre F. Malignant tumors of the central nervous system associated with familial polyposis of the colon: report of two cases. Dis Col Rect 1959;2:465-468. PMID 13839882.
  2. ^ Fauci,et al Harrison's Principle of Internal Medicine 16th Ed. p 2453
 This genetic disorder article is a stub. You can help Wikipedia by expanding it.
 This oncology article is a stub. You can help Wikipedia by expanding it.
Retrieved from "http://en.wikipedia.org../../../t/u/r/Turcot_syndrome.html"
In other languages