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[–] 4 points 2 years ago (1 child)

Another possibility is that she's XY, but the Y never activated, so she developed female but with a single "faulty" X chromosome.

I don't remember my biology classes well enough to say, but wouldn't that also mean that potentially neither of her parents were colorblind, since the Y would've come from her father while the faulty X would've come from her mother? And, if she were XY in this scenario, wouldn't that mean that she'd pass that trait along to her kids as well?

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  • [–] 4 points 2 years ago (1 child)

    if she were XY in this scenario, wouldn't that mean that she'd pass that trait along to her kids as well?

    I could be wrong, but I don’t believe XY females (Swyer syndrome) produce eggs and thus cannot bear their own children.

    But a colorblind XX woman who can bear children would give birth to colorblind sons and, if the father of the child is also colorblind, colorblind daughters.

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