Misattributed paternity

Misattributed paternity is the situation when a child’s putative father is not the child’s biological father. Misattributed paternity is not a rare phenomenon, its true incidence is not known, but medical students are routinely taught that the figure is in the 10 - 30% range.[1] Recent research suggests this figure may be too high, and the correct figure may be lower than five per cent, at least for Western Europe, North America and Australia.[2] Genetic testing for purposes other than establishing paternity has the potential to unintentionally yield information regarding a child’s paternity. This generally occurs in two different scenarios. The first and less complicated scenario occurs in searches for a suitable bone marrow or organ donor and the patient’s family members are tested. The second more controversial scenario is in the course of a genetic risk assessment for reproductive purposes.

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Misattributed paternity in organ donation

When misattributed paternity is exposed during the search for a suitable organ donor, it is ethically and legally acceptable to not disclose the information. This is because there are many reasons why the child would not make a suitable organ donor, and the fact of a non-match is not directly relevant to future reproductive or medical decisions.

Misattributed paternity in genetic counseling

In the context of a genetic risk assessment for reproductive purposes, a finding of misattributed paternity is more problematic, both ethically and legally. A classic example of this scenario is when a couple approaches a genetic counselor after the birth of a child with an autosomal recessive disorder, such as Tay Sachs, where both parents must be carriers of the trait. The test reveals that the father is not in fact a carrier and therefore cannot be the biological father, unless the disorder was caused by a mutation, which is a very negligible risk. The result is that instead of future children having a 25% chance of being affected, the chance is close to zero.

There are issues with the genetic counselor withholding the information, fully disclosing the misattributed paternity finding, partially disclosing the information, or attempting to address the issue before testing as part of the informed consent process.

Currently, there is no consensus on the appropriate approach a genetic counselor should take with respect to misattributed paternity, there are proponents for each approach. A 1983 report of the President’s Commission for the Study of Ethical Problems in Biomedicine and Behavioral Research recommends genetic counselor’s employ full disclosure. In contrast, in 1994 the Institute of Medicine’s Committee on Assessing Genetic Risks recommends that the genetic counselor disclose the information only to the mother. The Hereditary Disease Programme of the World Health Organization declared that there is probably never a situation in which the information should be disclosed to the presumed father.

Surveys of genetic counselors indicate that an overwhelming majority, 96 - 98.5%, would not divulge misattributed paternity results to the presumed father. In addition, only 60% would include information about misattributed paternity on an informed consent document. Therefore, genetic counseling custom appears to be in line with only telling the mother, or not disclosing misattributed paternity to either party. Courts often consider custom as evidence of what a reasonable physician would do in similar circumstances, which is the standard for medical malpractice.

Possible approaches

Notes

  1. ^ Michael Gilding (2005), 'Rampant Misattributed Paternity: The Creation of an Urban Myth,' in People and Place, Vol.13 No.2, page 1
  2. ^ Michael Gilding (2005), 'Rampant Misattributed Paternity: The Creation of an Urban Myth,' in People and Place, Vol.13 No.2, page 2

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