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akromyk

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About akromyk

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  1. Let's say we have a male with infertility issues. Him and his wife get a Chromosomal Analysis that comes back with his wife being fine, but him having: "balanced reciprocal translocation between chromosomes one and ten" 46,XY,t(1;10)(q21;q25.2) And the embryos from their first IVF round have the following abnormalities: 45,XY,dup(1)(q23q44),del(10)(q26),-22 46,XY,del(1)(q23),dup(10)(q26q26) Why would the embryos have duplications and deletions on the same chromosome but at different locations than the abnormalities in the potential father?
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