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From any possible resulting syndrome diseases, and conditions. As I mentioned earlier not all XXYâs will develop any or all these conditions. Since the extra X is just one of the 47 and thereâs a lot of other genetic material that can affect someone with this condition.
HOW COMMON IS IT??
This syndrome occurs in 1 to 1,000 approximately every so often...
        
        
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In live male births making its one of the most common chromosomal anomalies. This is identifying an individual through a Karyotype..
How it is transmitted.
You can find 23 pairs of chromosomes in each cell of the body. These cells contain factors that determine coloring, features, and sex. Women inherit two X-chromosomes, one from each parent, men on the other hand inherit on X-chromosomes one from of their mothers and a y chromosome from their father which brings us to how its transmitted...
        
        
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