I keep hearing people in the media talk about fixing errors in the genes for Huntington’s disease or cystic fibrosis in human embryos, but why wouldn’t you instead just screen for embryos without the disease-causing mutations? It is easier and probably far cheaper.
I do see therapeutic potential for genome editing of somatic cells for people with some diseases, especially ones affecting blood cells or other easily transplanted cells. And of course, CRISPR and other genome editing technologies will continue to be very, very useful in the lab to create model organisms and genetically modified cell lines. But for human embryos, I just don’t see a lot of upside to the technology.