Title of article
Germline mutations in MEN1 and BRCA1 genes in a woman with familial multiple endocrine neoplasia type 1 and inherited breast–ovarian cancer syndromes: a case report
Author/Authors
Papi، نويسنده , , Laura and Palli، نويسنده , , Domenico and Masi، نويسنده , , Laura and Putignano، نويسنده , , Anna Laura and Congregati، نويسنده , , Caterina and Zanna، نويسنده , , Ines and Marini، نويسنده , , Francesca and Giusti، نويسنده , , Francesca and Luzi، نويسنده , , Ettore and Tonelli، نويسنده , , Francesco and Genuardi، نويسنده , , Maurizio and Brandi، نويسنده , , Maria Luisa and Falch، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2009
Pages
5
From page
75
To page
79
Abstract
The simultaneous occurrence of mutations in two different tumor suppressor genes in the same individual is a very rare event. Here we report the case of a woman in whom germline mutations in both MEN1 and BRCA1 were identified. The severity of MEN1-related biochemical and clinical findings did not significantly differ from that for other affected family members lacking the BRCA1 mutation, except for the development of an extremely large visceral lipoma; the proband has not developed any BRCA1-related malignancies. We explore genetic and molecular rationales for an association between these neoplastic processes.
Journal title
Cancer Genetics and Cytogenetics
Serial Year
2009
Journal title
Cancer Genetics and Cytogenetics
Record number
1830011
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