z-logo
open-access-imgOpen Access
The Impact of Presymptomatic Molecular Testing in Hereditary Cancers
Author(s) -
Fiona MacDonald
Publication year - 2000
Publication title -
medical principles and practice
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.426
H-Index - 45
eISSN - 1423-0151
pISSN - 1011-7571
DOI - 10.1159/000054250
Subject(s) - medicine , hereditary cancer , genetic testing , cancer , oncology , breast cancer
Genetic factors are likely to be the primary determinants in around 5–10% of cancer patients. Over the last decade the identification of some of these cancer susceptibility genes has revolutionised our understanding of cancer in general. In addition, it has allowed us to improve our management of patients in those families with a genetic predisposition by offering presymptomatic testing and hence early intervention and treatment for the disease. This review will examine the major hereditary cancer syndromes and look at the tests currently available for their diagnosis. Molecular Changes Associated with the Development of Cancers

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom