Cargando…
A New de novo BRCA1 Mutation in a Young Breast Cancer Patient: A Case Report
BACKGROUND: BRCA1 and BRCA2 genes represent the most investigated breast and ovarian cancer predisposition genes. Ten cases of pathogenic de novo BRCA1 variations and six cases of pathogenic de novo BRCA2 variation have been reported at present. Here, we report a new case of a de novo BRCA1 gene mut...
Autores principales: | Scherz, Amina, Stoll, Susanna, Rothlisberger, Benno, Rabaglio, Manuela |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10184889/ https://www.ncbi.nlm.nih.gov/pubmed/37197323 http://dx.doi.org/10.2147/TACG.S405120 |
Ejemplares similares
-
Occurrence of variants of unknown clinical significance in genetic testing for hereditary breast and ovarian cancer syndrome and Lynch syndrome: a literature review and analytical observational retrospective cohort study
por: Adam, Felicia, et al.
Publicado: (2023) -
Eleven Years of Oncogenetic Consultations in a Swiss Center: Patient and Testing Characteristics
por: Grandjean, Bastien, et al.
Publicado: (2023) -
A new case of “de novo” BRCA1 mutation in a patient with early‐onset breast cancer
por: Antonucci, Ivana, et al.
Publicado: (2017) -
Novel de novo BRCA2 mutation in a patient with a family history of breast cancer
por: Hansen, Thomas V O, et al.
Publicado: (2008) -
A novel de novo BRCA1 mutation in a Chinese woman with early onset breast cancer
por: Kwong, Ava, et al.
Publicado: (2011)