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Article

[Turcot syndrome].

Nihon rinsho. Japanese journal of clinical medicine - 1 Jul 2000

Sunahara M, Nakagawara A

Abstract excerpt

Turcot syndrome is the association of colorectal polyposis with primary neuroepithelial tumors of the central nervous system such as glioblastoma and medulloblastoma. Including putative patients, more than 150 familial or sporadic cases of the syndrome have been reported in literature. Since early reports, there is considerable controversy regarding the modality of genetic transmission and the distinction from...

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Source

Identifiers

PMID: 10921328

Genes

FAP

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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[Turcot syndrome].PMID 10921328Read ↗

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A tale of four syndromes: familial adenomatous polyposis, Gardner syndrome, attenuated APC and Turcot syndrome.Semantic proximity Read ↗

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A novel APC gene mutation associated with a severe phenotype in a patient with Turcot syndrome.Semantic proximity Read ↗

Turcot's syndrome of glioma and polyposis occurs in the absence of germ line mutations of exons 5 to 9 of the p53 gene.Semantic proximity Read ↗

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Molecular analysis of astrocytoma associated with Turcot syndrome type 1--case report.Semantic proximity Read ↗

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