Literature DB >> 23464690

Genetic predisposition syndromes and their management.

David M Euhus1, Linda Robinson.   

Abstract

Apart from BRCA1, BRCA2, and TP53, more than a dozen breast cancer susceptibility genes have been identified. Recognizing affected individuals depends on evaluation of cancer family history and recognition of certain phenotypic markers on physical examination. Genetic testing provides a powerful tool for individualized risk stratification. Mutation carriers have several options for managing risk, including lifestyle alterations, enhanced surveillance, chemoprevention, and prophylactic surgery. Genetic counseling and testing should be considered in the initial evaluation of patients with newly diagnosed breast cancer because this information contributes to surgical decisions, radiation therapy options, and systemic therapy choices.
Copyright © 2013 Elsevier Inc. All rights reserved.

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Year:  2013        PMID: 23464690     DOI: 10.1016/j.suc.2013.01.005

Source DB:  PubMed          Journal:  Surg Clin North Am        ISSN: 0039-6109            Impact factor:   2.741


  12 in total

Review 1.  Genetic counseling for hereditary breast and ovarian cancer among Puerto Rican women living in the United States.

Authors:  Courtney L Scherr; Elsa Vasquez; Gwendolyn P Quinn; Susan T Vadaparampil
Journal:  Rev Recent Clin Trials       Date:  2014

2.  Genomic Disparities in Breast Cancer Among Latinas.

Authors:  Filipa Lynce; Kristi D Graves; Lina Jandorf; Charite Ricker; Eida Castro; Laura Moreno; Bianca Augusto; Laura Fejerman; Susan T Vadaparampil
Journal:  Cancer Control       Date:  2016-10       Impact factor: 3.302

3.  Provider discussion of genetic counseling among high-risk Spanish-preferring Latina breast cancer survivors.

Authors:  Claire C Conley; Jessica N Rivera Rivera; Eida M Castro-Figueroa; Laura Moreno; Julie Dutil; Jennifer D García; Charité Ricker; Gwendolyn P Quinn; Hatem Soliman; Susan T Vadaparampil
Journal:  Transl Behav Med       Date:  2022-10-07       Impact factor: 3.626

4.  Next-Generation Testing for Cancer Risk: Perceptions, Experiences, and Needs Among Early Adopters in Community Healthcare Settings.

Authors:  Kathleen R Blazer; Bita Nehoray; Ilana Solomon; Mariana Niell-Swiller; Julie O Culver; Gwen C Uman; Jeffrey N Weitzel
Journal:  Genet Test Mol Biomarkers       Date:  2015-11-05

Review 5.  Inductive and Deductive Approaches to Acute Cell Injury.

Authors:  Donald J DeGracia; Fika Tri Anggraini; Doaa Taha Metwally Taha; Zhi-Feng Huang
Journal:  Int Sch Res Notices       Date:  2014-10-13

6.  Comparison of multiple genotyping methods for the identification of the cancer predisposing founder mutation p.R337H in TP53.

Authors:  Mariana Fitarelli-Kiehl; Gabriel S Macedo; Rosane Paixão Schlatter; Patricia Koehler-Santos; Ursula da Silveira Matte; Patricia Ashton-Prolla; Juliana Giacomazzi
Journal:  Genet Mol Biol       Date:  2016-06-03       Impact factor: 1.771

7.  Transferring embryos with indeterminate PGD results: the ethical implications.

Authors:  Iris G Insogna; Elizabeth Ginsburg
Journal:  Fertil Res Pract       Date:  2016-02-01

8.  A pilot randomized trial of an educational intervention to increase genetic counseling and genetic testing among Latina breast cancer survivors.

Authors:  Claire C Conley; Eida M Castro-Figueroa; Laura Moreno; Julie Dutil; Jennifer D García; Carolina Burgos; Charité Ricker; Jongphil Kim; Kristi D Graves; Kimlin Tam Ashing; Gwendolyn P Quinn; Hatem Soliman; Susan T Vadaparampil
Journal:  J Genet Couns       Date:  2020-09-16       Impact factor: 2.537

9.  Development and pilot testing of a training for bilingual community education professionals about hereditary breast and ovarian cancer among Latinas: ÁRBOLES Familiares.

Authors:  Susan T Vadaparampil; Laura Moreno Botero; Lindsay Fuzzell; Jennifer Garcia; Lina Jandorf; Alejandra Hurtado-de-Mendoza; Claudia Campos-Galvan; Beth N Peshkin; Marc D Schwartz; Katherine Lopez; Charité Ricker; Katie Fiallos; Gwendolyn P Quinn; Kristi D Graves
Journal:  Transl Behav Med       Date:  2022-01-18       Impact factor: 3.626

10.  Screening for germline BRCA1, BRCA2, TP53 and CHEK2 mutations in families at-risk for hereditary breast cancer identified in a population-based study from Southern Brazil.

Authors:  Edenir Inêz Palmero; Bárbara Alemar; Lavínia Schüler-Faccini; Pierre Hainaut; Carlos Alberto Moreira-Filho; Ingrid Petroni Ewald; Patricia Koehler Dos Santos; Patricia Lisbôa Izetti Ribeiro; Cristina Brinkmann de Netto Oliveira; Florence Le Calvez-Kelm; Sean Tavtigian; Silvia Liliana Cossio; Roberto Giugliani; Maira Caleffi; Patricia Ashton-Prolla
Journal:  Genet Mol Biol       Date:  2016-05-24       Impact factor: 1.771

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