Abstract
During the last 5 years progress in molecular genetics has offered the possibility of genetic testing for inherited mutations of cancer-predisposing genes. The exact cellular function and carcinogenic potential of these genes is yet not completely understood. Only in 5-20% of all cancers inherited genetic mutations play an important role in the polygenic and multifactorial nature of the disease. Identification of inherited cancer syndromes, predictive generic testing, and counselling of women and family members at increased risk is of clinical importance. The debate surrounding presymptomatic diagnostic testing and adequate programmes for early cancer detection, prevention or clinical follow-up continues.
| Translated title of the contribution | Inherited cancer syndromes in gynaecology: What the practitioner needs to know! |
|---|---|
| Original language | German |
| Pages (from-to) | 362-375 |
| Number of pages | 14 |
| Journal | Schweizerische Medizinische Wochenschrift |
| Volume | 130 |
| Issue number | 10 |
| State | Published - 11 Mar 2000 |
| Externally published | Yes |
