Genetic Testing: Care, Consent, and Liability

Genetic Testing: Care, Consent, and Liability

Author(s): Neil F. Sharpe, Prof. Dr. Ronald F. Carter

Published Online: 4 JAN 2006

Print ISBN: 9780471649878

Online ISBN: 9780471748892

DOI: 10.1002/0471748897

About this Book

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A complete review of the issues with specific recommendations and guidelines.

With over 1,000 tests commercially available, genetic testing is revolutionizing medicine. Health care professionals diagnosing and treating patients today must consider genetic factors, the risks and limitations of genetic testing, and the relevant law. Genetic Testing: Care, Consent, and Liability offers the only complete, practical treatment of the genetic, clinical, ethical, and legal issue surrounding genetic testing. The authors present protocols, policies, and models of care that are currently in use, and explain the legal framework for genetic testing and counseling that has developed in North America, particularly with regard to the law of medical malpractice.

This essential book features an international roster of esteemed contributors including, Nancy P. Callanan, Bonnie S. LeRoy, Carole H. Browner, H. Mabel Preloran, Riyana Babul-Hirji, Cheryl Shuman, M.J. Esplen, Maren T. Scheuner, Dena S. Davis, JonBeckwith, Lisa Geller, Mark A. Hall, Andrew R. MacRae, David Chitayat, Roxanne Mykitiuk, Stephanie Turnham, Mireille Lacroix, Jinger G, Hoop, Edwin H, Cook, Jr., S. H. Dinwiddie, Elliot S. Gershon, C. Anthony Rupar, Lynn Holt, Bruce R. Korf, Anne Summers, S. Annie Adams, Daniel L. Van Dyke, Rhett P. Ketterling, Erik C. Thorland, Timothy Caulfield, Lorraine Sheremeta, Richard Gold, Jon F. Merz, David Castle, Peter J. Bridge, JS Parboosingh, Patricia T. Kelly, Julianne M. O'Daniel, Allyn McConkie-Rosell, Beatrice Godard, Bartha Maria Knoppers, David Weisbrot.

The coverage also includes:
* Genetic screening, including prenatal, neonatal, carrier, and susceptibility testing
* Diagnosis, risk assessment, confidentiality, and clinical/legal issues related to follow-up
* Interpreting test results and communicating them to patients
* psychological considerations
* Informed consent
* Family history evaluations
* Referral to medical geneticists and genetic counselors


Genetic Testing Care, Consent, and Liability is a must-have resource for clinical geneticists, genetic counselors, specialists, family physicians, nurses, public health professionals, and medical students.

Table of contents

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    2. Chapter 2

      Communication (pages 24–52)

      C. H. Browner, H. Mabel Preloran, Riyana Babul-Hirji and Cheryl Shuman

    3. Chapter 7

      Informed Consent (pages 128–162)

      Jon Beckwith, Lisa Geller and Mark A. Hall

    4. Chapter 8

      Prenatal and Neonatal Screening (pages 163–218)

      Andrew R. MacRae, David Chitayat, Roxanne Mykitiuk, Mireille Lacroix and Stephanie Turnham

    5. Chapter 9

      Genetics of Common Neurological Disorders (pages 219–237)

      Jinger G. Hoop, Edwin H. Cook, Stephen H. Dinwiddie and Elliot S. Gershon

    6. Chapter 10

      Carrier Screening (pages 238–267)

      C. Anthony Rupar, Lynn Holt and Bruce R. Korf

    7. Chapter 12

      Test Samples and Laboratory Protocols (pages 292–339)

      S. Annie Adams, Daniel L. Van Dyke, Rhett P. Ketterling, Erik C. Thorland, Timothy Caulfield, Lorraine Sheremeta, E. Richard Gold, Jon F. Merz and David Castle

    8. Chapter 13

      Risk Assessment (pages 340–354)

      Peter J. Bridge and Jillian S. Parboosingh

    9. Chapter 14

      Test Results: Communication and Counseling (pages 355–397)

      Julianne M. O'daniel, Allyn McConkie-Rosell and Patricia T. Kelly

    10. Chapter 15

      Confidentiality and Recall (pages 398–424)

      B′eatrice Godard, Bartha-Maria Knoppers, Alasdair Hunter, Neil F. Sharpe, Michelle Mullen and W. S. Meschino

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