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There is technologies to diagnose this, one is a chromosome analysis. We can determine if there ia an extra chromosome here in the male. There is no cure but the symptoms can be reduced by:
It is present at birth and an error happens during sperm or embryo formation. Occurs when an extra chromosome is added so it the male is XYY and has a total of 47 chromosomes. It is a mutation, it is not inherited.
This syndrome only appears in the male population. It occurs every 1 in 1000 births and is quite rare. SOmetimes it goes unnoticed, so only 25% are ever diagnosed.