Literature DB >> 21343792

Committee Opinion No. 478: Family history as a risk assessment tool.

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Abstract

Family history plays a critical role in assessing the risk of inherited medical conditions and single gene disorders. Several methods have been established to obtain family medical histories, including the family history questionnaire or checklist and the pedigree. The screening tool selected should be tailored to the practice setting and patient population. It is recommended that all women receive a family history evaluation as a screening tool for inherited risk. Family history information should be reviewed and updated regularly, especially when there are significant changes to family history. Where appropriate, further evaluation should be considered for positive responses, with referral to genetic testing and counseling as needed.

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Year:  2011        PMID: 21343792     DOI: 10.1097/AOG.0b013e318214780e

Source DB:  PubMed          Journal:  Obstet Gynecol        ISSN: 0029-7844            Impact factor:   7.661


  8 in total

Review 1.  What characterizes cancer family history collection tools? A critical literature review.

Authors:  J E Cleophat; H Nabi; S Pelletier; K Bouchard; M Dorval
Journal:  Curr Oncol       Date:  2018-08-14       Impact factor: 3.677

Review 2.  Genomics and perinatal care.

Authors:  Joann Bodurtha; Jerome F Strauss
Journal:  N Engl J Med       Date:  2012-01-05       Impact factor: 91.245

3.  Preconception counseling: do patients learn about genetics from their obstetrician gynecologists?

Authors:  Adrienne H Mandelberger; Jared C Robins; John E Buster; William C Strohsnitter; Beth J Plante
Journal:  J Assist Reprod Genet       Date:  2015-06-09       Impact factor: 3.412

4.  Evaluation of a novel electronic genetic screening and clinical decision support tool in prenatal clinical settings.

Authors:  Emily A Edelman; Bruce K Lin; Teresa Doksum; Brian Drohan; Vaughn Edelson; Siobhan M Dolan; Kevin Hughes; James O'Leary; Lisa Vasquez; Sara Copeland; Shelley L Galvin; Nicole DeGroat; Setul Pardanani; W Gregory Feero; Claire Adams; Renee Jones; Joan Scott
Journal:  Matern Child Health J       Date:  2014-07

5.  Genetic risk.

Authors:  Leo P Ten Kate
Journal:  J Community Genet       Date:  2012-08-15

6.  Web-based surveillance of public information needs for informing preconception interventions.

Authors:  Angelo D'Ambrosio; Eleonora Agricola; Luisa Russo; Francesco Gesualdo; Elisabetta Pandolfi; Renata Bortolus; Carlo Castellani; Faustina Lalatta; Pierpaolo Mastroiacovo; Alberto Eugenio Tozzi
Journal:  PLoS One       Date:  2015-04-16       Impact factor: 3.240

Review 7.  Changing trends in carrier screening for genetic disease in the United States.

Authors:  Shivani B Nazareth; Gabriel A Lazarin; James D Goldberg
Journal:  Prenat Diagn       Date:  2015-07-27       Impact factor: 3.050

Review 8.  Executive Summary of the Early-Onset Breast Cancer Evidence Review Conference.

Authors:  David Chelmow; Mark D Pearlman; Amy Young; Laura Bozzuto; Sandra Dayaratna; Myrlene Jeudy; Mallory E Kremer; Dana Marie Scott; Julia Sage O'Hara
Journal:  Obstet Gynecol       Date:  2020-06       Impact factor: 7.623

  8 in total

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