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Reduced life expectancy seen in hereditary diseases which predispose to early-onset tumors
Author(s) -
D. Gareth Evans,
Sarah Ingham
Publication year - 2013
Publication title -
the application of clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.879
H-Index - 32
ISSN - 1178-704X
DOI - 10.2147/tacg.s35605
Subject(s) - medicine , neurofibromatosis , disease , familial adenomatous polyposis , life expectancy , hereditary diseases , lynch syndrome , cancer , heredity , age of onset , pediatrics , phenocopy , genetic disorder , pathology , colorectal cancer , genetics , dna mismatch repair , population , biology , gene , mutant , environmental health
There are several hereditary diseases that are a predisposition to early-onset tumors. These include syndromic conditions like neurofibromatosis 1 and 2, von Hippel-Lindau syndrome, Gorlin syndrome, multiple endocrine neoplasia, and familial adenomatous polyposis; and conditions which are usually not possible to diagnose clinically in a single individual, such as Lynch syndrome and BRCA1/2. Understanding of the mortality in hereditary cancer predisposing diseases is important for developing effective disease treatment programs. A number of studies have been undertaken to investigate the genetic predictors, prevalence and incidence, and treatment outcomes of these diseases; however, the majority examine only the most common of these diseases (eg, neurofibromatosis or BRCA), or look into postoperative survival. The mortality of individuals who are diagnosed with one of these hereditary diseases remains an area for investigation. This review is the first to attempt identification of studies investigating life expectancy in hereditary diseases which predispose to early-onset tumors.

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