In dieser Arbeit wird anhand eines Würzburger Studienkollektivs von erblich an Brust-und Ovarialkrebs Erkrankten, das 150 Ratsuchende umfasst, das Risikokalkulationsprogramm Cyrillic 2.13 zur Abschätzung von Mutations- und Erkrankungswahrscheinlichkeiten bei erblichem Brust- und Ovarialkrebs untersucht. Es werden die vom Programm berechneten Mutationswahrscheinlichkeiten mit dem tatsächlichen Mutationsstatus der Probanden verglichen. Außerdem werden Stammbäume der Probanden auf Angehörige 1. und 2. Generation gekürzt, um zu untersuchen, ob dies die errechneten Ergebnisse beeinflusst. Es zeigt sich hierbei jedoch kein signifikanter Unterschied. / The risk calculating programme Cyrillic 2.13 for the likeliness of developing hereditary breast- and ovarian cancer is being examined in 150 Probands of Würzburg who had already been tested for mutations in brca -genes. It was known whether they had or did not have a mutation. The results are being compared to those calculated by Cyrillic 2.13 depending on their pedegree. The probands' pedigrees then were reduced to only first- and second degree relatives in order to figure out whether there is an influence on the calculated mutation rate or not. The results show, that there is no significant difference between the mutation rates offered by the programme compared to those tested for the probands.
Identifer | oai:union.ndltd.org:uni-wuerzburg.de/oai:opus.bibliothek.uni-wuerzburg.de:5294 |
Date | January 2010 |
Creators | Meyer, Johanna |
Source Sets | University of Würzburg |
Language | deu |
Detected Language | English |
Type | doctoralthesis, doc-type:doctoralThesis |
Format | application/pdf |
Rights | https://opus.bibliothek.uni-wuerzburg.de/doku/lic_ohne_pod.php, info:eu-repo/semantics/openAccess |
Page generated in 0.0023 seconds