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Memorial University - Electronic Theses and Dissertations 5
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Document Description
TitleClinical and genealogical studies of familial colorectal cancer type-x in Newfoundland
AuthorHarnett, David
DescriptionThesis (M.Sc.)--Memorial University of Newfoundland, 2011. Medicine
Date2011
Paginationxii, 130 leaves : ill. (chiefly col.), col. maps
SubjectColon (Anatomy)--Cancer--Susceptibility--Newfoundland and Labrador--Case studies; Rectum--Cancer--Susceptibility--Newfoundland and Labrador--Case studies; Colon (Anatomy)--Cancer--Newfoundland and Labrador--Genetic aspects; Rectum--Cancer--Newfoundland and Labrador--Genetic aspects; Genealogy--Health aspects
Subject.MESHColorectal Neoplasms--Newfoundland and Labrador; Colorectal Neoplasms--genetics--Newfoundland and Labrador; Disease Susceptibility--Newfoundland and Labrador
DegreeM.Sc.
Degree GrantorMemorial University of Newfoundland. Faculty of Medicine
DisciplineMedicine
LanguageEng
Spatial CoverageCanada--Newfoundland and Labrador
NotesBibliography: leaves 102-116.
AbstractFamilial Colorectal Cancer Type-X (FCCTX) is a syndrome defined by criteria used to identify Lynch Syndrome, but in which the genetic cause is not the result of mismatch repair (MMR) gene mutations with the genetic etiology remaining unknown. In an attempt to facilitate novel gene discovery in FCCTX, families (N = 12) were identified with a strong family history of CRC (≥5 cases of CRC) of unknown genetic etiology, who fulfilled the criteria for FCCTX: meeting the ACI, possessing no known MMR gene mutation, and a probands with MSS CRC. Significant variability was found in terms of age of onset, tumour location, and genetic profile of CRCs amongst the probands of these families. First-degree relatives of the probands of the FCCTX families (N = 126) were compared as a group to first-degree relatives of the probands of fifteen Lynch Syndrome families (N = 153). No difference in lifetime risk of CRC existed between the groups, but the families fulfilling the FCCTX criteria demonstrated a significantly later onset of CRC and fewer cases of extra-colonic cancers. Mapping locations of origin demonstrated that families originated from multiple different geographic isolates. The use of a customized hereditability database failed to demonstrate genealogical linkages between the twelve FCCTX families. In six of the FCCTX families, further archival research also failed to yield a direct link. The heterogeneous clinical and pathological features, geographic distribution of probands in different isolates, and failure to identify genealogical linkages between families suggest that multiple genes underlie the susceptibility to CRC observed in FCCTX.
TypeText
Resource TypeElectronic thesis or dissertation
FormatImage/jpeg; Application/pdf
SourcePaper copy kept in the Centre for Newfoundland Studies, Memorial University Libraries
RightsThe author retains copyright ownership and moral rights in this thesis. Neither the thesis nor substantial extracts from it may be printed or otherwise reproduced without the author's permission.
CollectionElectronic Theses and Dissertations
Scanning StatusCompleted
PDF File(15.60 MB) -- http://collections.mun.ca/PDFs/theses/Harnett_David.pdf
CONTENTdm file name20285.cpd