Klinefelter syndrome is characterised by the presence of a total of 47 chromosomes instead of 46 due to an extra copy of X chromosome. It may result from the non-disjunction of sex chromosomes during the formation of either male or female gamete. The chromosomal complement of this syndrome is 44 XXY.
Symptoms: Klinefelter syndrome person is phenotypically male with low levels of testosterone, gynaecomastia, reduced body and facial hair and decresed ability or total inability to produce spermatozoa.