Final answer:
In the case of an XXY offspring with Klinefelter Syndrome exhibiting a pointed nose, a nondisjunction event in one of the parents during gametogenesis caused the condition, with a carrier parent providing the recessive allele for the pointed nose.
Step-by-step explanation:
The question revolves around a genetic nondisjunction event that leads to Klinefelter Syndrome (XXY) and the inheritance of an X-linked trait for nose shape, where round nose is dominant over pointed nose. Considering that both XY parent with a round nose and XX parent with a round nose have produced an XXY offspring with a pointed nose, we can infer that one parent must have carried at least one X chromosome with a recessive allele for a pointed nose (Xp). The occurrence of Klinefelter Syndrome suggests a nondisjunction event during gametogenesis in one of the parents. Nondisjunction might have happened in the father during meiosis I, where both X and Y chromosomes went to the same sperm, or in the mother when the two X chromosomes failed to separate, leading to an egg with two X chromosomes, one of which carried the recessive allele (XpX).