BRCA1/2-related breast cancers (BC) can be considered a separate entity compared to sporadic ones. Current knowledge suggests that the overall management is different. Herein, the different topics of management of BRCA1/2-associated BC are considered including cancer genetic counseling, surveillance, chemoprevention, prophylactic surgery, oncological treatment and psychosocial aspects. Cancer genetic counseling is a specific modality for the management of at-risk subjects that foresees a multidisciplinary approach and patientsfocused interventions. An integrated multidisciplinary approach in cancer genetic counseling (CGC) is required to support women with high inherited risk of developing hereditary cancers in the complex decisions r...
The discovery of the association between breast and ovarian cancer and the BRCA genes and the develo...
Hereditary breast cancers, mainly due to BRCA1 and BRCA2 mutations, account for only 5–10% of this d...
Introduction.Breast cancer gene 1 and 2 (BRCA1/2) mutation carriers are at a higher risk of developi...
BRCA1/2-related breast cancers (BC) can be considered a separate entity compared to sporadic ones. C...
Germline mutations in BRCA1/BRCA2 significantly increase the risk of breast and ovarian cancer in wo...
Sarah Edaily, Hikmat Abdel-Razeq Department of Internal Medicine, King Hussein Cancer Center, Amman,...
Cancer survivors harboring inherited pathogenic variants in the breast cancer (BC) susceptibility ge...
PURPOSE: To develop recommendations for management of patients with breast cancer (BC) with germline...
Mutations due to hereditary related genes such as BRCA1, BRCA2, TP53 and PTEN confer greater risk of...
Individuals who carry an inherited mutation in the breast cancer 1 (BRCA1) and BRCA2 genes have a si...
Abstract: A consensus conference including thirty experts was held in April, 2007, to discuss risk f...
ImportancePotentially harmful mutations of the breast cancer susceptibility 1 and 2 genes (BRCA1/2) ...
Genetic counseling and BRCA1/BRCA2 genes testing are routinely offered in a clinical setting. Howeve...
Pathogenic mutations in two autosomal dominant genes, BRCA1 and BRCA2 , with high penetrance are ...
One in 8 women will be diagnosed with breast cancer in her lifetime, but only 5-10% of women who are...
The discovery of the association between breast and ovarian cancer and the BRCA genes and the develo...
Hereditary breast cancers, mainly due to BRCA1 and BRCA2 mutations, account for only 5–10% of this d...
Introduction.Breast cancer gene 1 and 2 (BRCA1/2) mutation carriers are at a higher risk of developi...
BRCA1/2-related breast cancers (BC) can be considered a separate entity compared to sporadic ones. C...
Germline mutations in BRCA1/BRCA2 significantly increase the risk of breast and ovarian cancer in wo...
Sarah Edaily, Hikmat Abdel-Razeq Department of Internal Medicine, King Hussein Cancer Center, Amman,...
Cancer survivors harboring inherited pathogenic variants in the breast cancer (BC) susceptibility ge...
PURPOSE: To develop recommendations for management of patients with breast cancer (BC) with germline...
Mutations due to hereditary related genes such as BRCA1, BRCA2, TP53 and PTEN confer greater risk of...
Individuals who carry an inherited mutation in the breast cancer 1 (BRCA1) and BRCA2 genes have a si...
Abstract: A consensus conference including thirty experts was held in April, 2007, to discuss risk f...
ImportancePotentially harmful mutations of the breast cancer susceptibility 1 and 2 genes (BRCA1/2) ...
Genetic counseling and BRCA1/BRCA2 genes testing are routinely offered in a clinical setting. Howeve...
Pathogenic mutations in two autosomal dominant genes, BRCA1 and BRCA2 , with high penetrance are ...
One in 8 women will be diagnosed with breast cancer in her lifetime, but only 5-10% of women who are...
The discovery of the association between breast and ovarian cancer and the BRCA genes and the develo...
Hereditary breast cancers, mainly due to BRCA1 and BRCA2 mutations, account for only 5–10% of this d...
Introduction.Breast cancer gene 1 and 2 (BRCA1/2) mutation carriers are at a higher risk of developi...