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The Use of a Diagnostic Database in Clinical Oncogenetics

In addition to a relatively small number of well known hereditary cancer syndromes, hundreds of presumed or proven hereditary disorders have been observed to manifest cancer as a characteristic feature or as a possible complication. The recognition of these disorders may be of great importance for t...

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Detalles Bibliográficos
Autores principales: Sijmons, Rolf H, Burger, Gerard TN
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2840010/
http://dx.doi.org/10.1186/1897-4287-1-1-31
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author Sijmons, Rolf H
Burger, Gerard TN
author_facet Sijmons, Rolf H
Burger, Gerard TN
author_sort Sijmons, Rolf H
collection PubMed
description In addition to a relatively small number of well known hereditary cancer syndromes, hundreds of presumed or proven hereditary disorders have been observed to manifest cancer as a characteristic feature or as a possible complication. The recognition of these disorders may be of great importance for the medical management of the families involved. Specialized databases, like the Familial Cancer Database (FaCD, http://www.facd.info), may be helpful in the making of differential diagnoses and offer advantages compared with traditional textbooks and on-line literature searches. Based on our own experience and interviews with the other Dutch family cancer clinics, we expect that in similar clinics, computer-assisted differential diagnosis will be primarily used in helping to decide whether or not cancer patients and families should be referred to family cancer clinics for further study and counseling. FaCD has been developed as a tool for experts. As general practitioners and other health professionals with non-expert knowledge of cancer genetics are under increasing pressure to advise on genetic risks, it should be encouraged that other software is developed to support them in interpreting family histories of cancer.
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spelling pubmed-28400102010-03-17 The Use of a Diagnostic Database in Clinical Oncogenetics Sijmons, Rolf H Burger, Gerard TN Hered Cancer Clin Pract Research In addition to a relatively small number of well known hereditary cancer syndromes, hundreds of presumed or proven hereditary disorders have been observed to manifest cancer as a characteristic feature or as a possible complication. The recognition of these disorders may be of great importance for the medical management of the families involved. Specialized databases, like the Familial Cancer Database (FaCD, http://www.facd.info), may be helpful in the making of differential diagnoses and offer advantages compared with traditional textbooks and on-line literature searches. Based on our own experience and interviews with the other Dutch family cancer clinics, we expect that in similar clinics, computer-assisted differential diagnosis will be primarily used in helping to decide whether or not cancer patients and families should be referred to family cancer clinics for further study and counseling. FaCD has been developed as a tool for experts. As general practitioners and other health professionals with non-expert knowledge of cancer genetics are under increasing pressure to advise on genetic risks, it should be encouraged that other software is developed to support them in interpreting family histories of cancer. BioMed Central 2003-01-15 /pmc/articles/PMC2840010/ http://dx.doi.org/10.1186/1897-4287-1-1-31 Text en
spellingShingle Research
Sijmons, Rolf H
Burger, Gerard TN
The Use of a Diagnostic Database in Clinical Oncogenetics
title The Use of a Diagnostic Database in Clinical Oncogenetics
title_full The Use of a Diagnostic Database in Clinical Oncogenetics
title_fullStr The Use of a Diagnostic Database in Clinical Oncogenetics
title_full_unstemmed The Use of a Diagnostic Database in Clinical Oncogenetics
title_short The Use of a Diagnostic Database in Clinical Oncogenetics
title_sort use of a diagnostic database in clinical oncogenetics
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2840010/
http://dx.doi.org/10.1186/1897-4287-1-1-31
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