Breast Cancer
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Contents
1 Primary Author(s)*
2 Graphical Data
2 General Disease Overview / Description of Cancer Category
3 WHO Classification Pages (Includes Links to Content)
4 Other Related Pages (Includes Links to Content)
5 Additional Information 6 References
6.1 EXAMPLE Book
6.2 EXAMPLE Journal Article
7 Notes
Primary Author(s)*
Put your text here
Graphical Data Links
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Table 5: Genes with known hereditary risk associations in breast cancer according to National Comprehensive Cancer Network (NCCN) Guidelines (version 3.2019)
| Gene | Associated Syndrome; Breast Cancer Subtype |
| ATM | Ataxia telangiectasia syndrome |
| BRCA1 | BRCA-Related Breast/ Ovarian Cancer Syndrome; TNBC |
| BRCA2 | BRCA-Related Breast/ Ovarian Cancer Syndrome; TNBC |
| CDH1 | Hereditary Diffuse Gastric Cancer and Lobular Breast Cancer |
| CHEK2 | Inherited breast cancer |
| NBN | Nijmegen Breakage Syndrome (autosomal recessive inheritance) |
| NF1 | Neurofibromatosis type 1 |
| PALB2 | Fanconi anemia |
| PTEN | Cowden syndrome |
| STK11 | Peutz-Jeghers syndrome |
| TP53 | Li-Fraumeni syndrome |
Inheritance is autosomal dominant with incomplete penetrance, unless otherwise specified
General Disease Overview / Description of Cancer Category
Put your text here
WHO Classification Pages
(Includes Links to Content)
Put your text here, EXAMPLE #Chromophobe renal cell carcinoma
Other Related Pages
(Includes Links to Content)
Put your text here, EXAMPLE #Acute Myeloid Leukemia (AML) with Mutated FLT3
Additional Information
Put your text here
References
EXAMPLE Book Arber DA, et al., (2008). Acute myeloid leukaemia with recurrent genetic abnormalities, in World Health Organization Classification of Tumours of Haematopoietic and Lymphoid Tissues, 4th edition. Swerdlow SH, Campo E, Harris NL, Jaffe ES, Pileri SA, Stein H, Thiele J, Vardiman JW, Editors. IARC Press: Lyon, France, p117-118.
EXAMPLE Journal Article Li Y, et al., (2001). Fusion of two novel genes, RBM15 and MKL1, in the t(1;22)(p13;q13) of acute megakaryoblastic leukemia. Nat Genet 28:220-221, PMID 11431691.
Notes
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