Utvidet returrett til 31. januar 2025

Descriptive and analytical epidemiology of breast cancer

Om Descriptive and analytical epidemiology of breast cancer

Breast cancer is the first cancer of women in the world and in Tunisia. Its incidence is in continuous rise.The risk factors of breast cancer are multiple. There are endogenous and exogenous hormonal factors, factors related to reproduction, demographic and breast factors, environmental factors and hereditary factors. Although the majority of cases are sporadic, it is estimated that 5-10% of cases have an inherited component. Two major susceptibility genes have been identified, BRCA1 (Breast CAncer 1) and BRCA2 (Breast CAncer 2), which play a key role in the DNA error repair process. Constitutional deleterious mutations in BRCA1 and BRCA2 are associated with a high risk of developing breast cancer, which reinforces the interest in identifying these mutations in families at risk.

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  • Språk:
  • Engelsk
  • ISBN:
  • 9786205899809
  • Bindende:
  • Paperback
  • Sider:
  • 72
  • Utgitt:
  • 15. april 2023
  • Dimensjoner:
  • 150x5x220 mm.
  • Vekt:
  • 125 g.
  • BLACK NOVEMBER
  Gratis frakt
Leveringstid: 2-4 uker
Forventet levering: 21. desember 2024
Utvidet returrett til 31. januar 2025

Beskrivelse av Descriptive and analytical epidemiology of breast cancer

Breast cancer is the first cancer of women in the world and in Tunisia. Its incidence is in continuous rise.The risk factors of breast cancer are multiple. There are endogenous and exogenous hormonal factors, factors related to reproduction, demographic and breast factors, environmental factors and hereditary factors. Although the majority of cases are sporadic, it is estimated that 5-10% of cases have an inherited component. Two major susceptibility genes have been identified, BRCA1 (Breast CAncer 1) and BRCA2 (Breast CAncer 2), which play a key role in the DNA error repair process. Constitutional deleterious mutations in BRCA1 and BRCA2 are associated with a high risk of developing breast cancer, which reinforces the interest in identifying these mutations in families at risk.

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