Named for the mythical monster with a lion’s head, a goat’s body and the tail of a snake, human chimeras have two or more genetically distinct types of cells in their bodies. This anomaly is thought to be caused by the absorption, or fusing, of twins before they are born. This would cause the chimera to carry two sets of DNA in their body. One set of their DNA and one that would have been their twin’s DNA. This second set of DNA can show up anywhere in the body. A second, distinct set of DNA may be present in the skin, blood, or even reproductive organs of the chimera. This was what happened in the case of Lynda Fairchild, profiled in the ABC documentary.
Fairchild underwent DNA maternity testing shortly after the birth of her child. Results showed a poor match, as if she was the baby’s grandmother. It was concluded that Fairchild may have been a chimera, her body the result of the fusion of two non identical embryos at the earliest stage of development. Different parts of her body could have come from different cell lines. Further testing indicated that cells taken from her reproductive organs, contained different DNA than those taken from her mouth for the DNA testing and were a match to her children.
Though cases like this are often given a lot of press, their occurrence is very rare. No one knows exactly how many cases of human chimera there are, but most studies cite only 30 reported cases in all of human history.
What Does This Mean For My DNA Paternity Test Results?
An inclusion, or “positive” DNA paternity test shows that an alleged father and the child share the same DNA. Therefore that man is considered to be the biological father. The father’s DNA was passed to the child, and the loci (markers) all match up. It’s virtually impossible (that is, very, very unlikely) that possessing two sets of DNA would make someone appear to be a father when they are not. Matches at all locations indicate a positive paternity test result, even if the father is a chimera.
An exclusion (when a man is not the father of a child) could potentially be affected, by someone being a chimera. It is possible for a chimera to pass one set of DNA on to their child but show a second set of DNA with a cheek swab, as in the Linda Fairchild case. Even so, the child and the father would still likely show a partial match, similar to that of a child and an uncle, since the second set of DNA would be that of the father’s unborn twin.
If you’re looking for more information on Tetragametic Chimerism, we have included some great links to help you get started on your search. Disputed Maternity Leads to Identification of Tetragametic Chimerism – The New England Journal of Medicine,Genetic Mosaics
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