Is Polydactyly a Harmless Genetic Mutation or a Problem?

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The discussion centers on the condition known as polydactyly, where individuals are born with extra fingers. It is noted that this trait can be inherited dominantly, meaning that typically one parent will also have extra digits. In most cases, polydactyly is not associated with any genetic disease and does not impede normal life. However, there are instances where polydactyly may be linked to other genetic disorders, which can present additional symptoms or abnormalities. The conversation highlights the distinction between harmless mutations and inherited traits, emphasizing that while polydactyly itself is generally benign, it can sometimes indicate a more complex genetic issue.
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Just to ask professional researchers a question,
Normally, human beings are born to have ten fingers, but I noticed long ago some friends of mine in my hometown have twelve whereas their parents are normally with ten only. This I assume is a genetic problem which the bad gene (6 fingers on one hand) from a parent gets combined with another from the other parent. So how can we conclude such a case is not a harmless mutation ? Even though with twelve fingers, still they can lead normal lives anyway. I think it is a harmless mutation if that poeple can call mutation instead of genetic inheritance.

Thamnk you
 
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The condition of having extra digits is called polydactyly. I am not sure what you mean with your last comment, you mean a spontaneous mutation vs an inherited mutation? Or a single mutation vs genetic disease?

Familial polydactyly occurs as a dominantly inherited trait, meaning that one of the parents will also have extra digits, in most cases this does not indicate a genetic disease: you only have an extra finger.

There are cases were polydactyly is associated with other genetic disorders or syndroms, where other symptoms or abnormalities are present.
 
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