Difference between revisions of "Hereditary breast cancer"

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! Gene
! Gene
! Syndrome
! Syndrome
! Other cancers
! Cancers
! Notes
! Notes
|-
|-
| BRCA1
| BRCA1
| Familial breast and ovarian cancer<ref name=omim113705>{{OMIM|113705}}</ref>
| Familial breast and ovarian cancer<ref name=omim113705>{{OMIM|113705}}</ref>
| male breast, ovarian, prostate, pancreas, fallopian tube
| breast, male breast, ovarian, prostate, pancreas, fallopian tube
| younger individuals vis-à-vis BRCA2
| younger individuals vis-à-vis BRCA2
|-
|-
| BRCA2
| BRCA2
| Familial breast and ovarian cancer 2<ref name=omim600185>{{OMIM|600185}}</ref>
| Familial breast and ovarian cancer 2<ref name=omim600185>{{OMIM|600185}}</ref>
| male breast, ovarian, prostate, pancreas, stomach, melanoma, gallbladder, bile duct, pharynx
| breast, male breast, ovarian, prostate, pancreas, stomach, melanoma, gallbladder, bile duct, pharynx
| older individuals vis-à-vis BRCA1
| older individuals vis-à-vis BRCA1
|-  
|-  
| TP53 (p53)
| TP53 (p53)
| [[Li-Fraumeni syndrome]] ([[AKA]] ''SBLA syndrome'')
| [[Li-Fraumeni syndrome]] ([[AKA]] ''SBLA syndrome'')
| [[sarcoma]]s, brain cancer, larynx, lung, leukemia, [[adrenal cortical carcinoma]]
| [[sarcoma]]s, brain, larynx, lung, leukemia, [[adrenal cortical carcinoma|adrenal]], breast
| often present in childhood
| often present in childhood
|-
|-
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| STK11
| STK11
| [[Peutz-Jeghers syndrome]]
| [[Peutz-Jeghers syndrome]]
| breast cancer, GI cancer, [[Sertoli cell tumour]], [[Granulosa cell tumour]], [[SCTAT]]
| breast, gastrointestinal, [[Sertoli cell tumour]], [[granulosa cell tumour]], [[SCTAT]]
| characteristic GI [[hamartoma]]s, mucocutaneous pigmentation
| characteristic GI [[hamartoma]]s, mucocutaneous pigmentation
|-
|-
| PTEN
| PTEN
| [[Cowden syndrome]]
| [[Cowden syndrome]]
| breast, thyroid (PTC), endometrial, renal, colorectal
| breast, thyroid ([[papillary thyroid carcinoma|PTC]]), endometrial, renal, colorectal
| -
| -
|-
|-
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