Cargando…
A Paternally Inherited BRCA1 Mutation Associated with an Unusual Aggressive Clinical Phenotype
This report highlights the necessity of genetic testing, at least for BRCA1 mutations, of young females diagnosed with triple negative breast cancer, even in the absence of or limited family history. A 34-year-old female with a locally advanced, triple negative tumour, which perforated the skin, is...
Autores principales: | Fostira, Florentia, Tsoukalas, Nikolaos, Konstantopoulou, Irene, Georgoulias, Vassilios, Christophyllakis, Charalambos, Yannoukakos, Drakoulis |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3934306/ https://www.ncbi.nlm.nih.gov/pubmed/24660075 http://dx.doi.org/10.1155/2014/875029 |
Ejemplares similares
-
A Patient Affected with Serous Ovarian/Peritoneal Carcinoma Carrying the FANCM Mutation
por: Nikolaidi, Adamantia, et al.
Publicado: (2019) -
Mutational spectrum of APC and genotype-phenotype correlations in Greek FAP patients
por: Fostira, Florentia, et al.
Publicado: (2010) -
Prevalence of BRCA1 Mutations in Familial and Sporadic Greek Ovarian Cancer Cases
por: Stavropoulou, Alexandra V., et al.
Publicado: (2013) -
Correction: Prevalence of BRCA1 Mutations in Familial and
Sporadic Greek Ovarian Cancer Cases
por: Stavropoulou, Alexandra V., et al.
Publicado: (2013) -
Contribution of BRCA1 germ-line mutations to breast cancer in Greece: a hospital-based study of 987 unselected breast cancer cases
por: Armaou, S, et al.
Publicado: (2009)