Familial Brain Tumour
Looking for causes
Since 2003, the Deutsche Hirntumorhilfe keeps a register about genetically related gliomas. The outcomes of the working group shows, that the percentage of affected adults is expected to be about 2%. This is why continuous recording of additional cases is very important in order to explore a possible inheritance of gliomas or even to identify environmental factors that might cause brain tumours.
Scientists are involved in researching the mechanisms of the disease's development worldwide in order to identify causes and risks for brain tumour growth. According to a research group at the University of Texas, 5 to 10% of the occurring cases seem to be hereditary, but it is not sure which genes are the supporters of this disease.
The National Cancer Institute spent 11 million U.S. Dollars on the gliogene study, a project where researchers are trying to find genetic risk factors for the development of malignant brain tumours including glioblastoma. There are 15 participating research centres recruiting patients for the largest genetic study on causes and risks of glioma. Investigating at least 400 families with two or more parties of a primary malignant brain tumour, the study aims to identify genetic links between the family members. Cross-links of that type might provide important key information about the disease and thus contribute to improving the treatment and the development of preventive measures.
If there are two or more patients with glioma within your primary related family members, please contact us by dialling 0049.3437.702 702.
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