XXY syndrome (also called Klinefelter syndrome), was first described in 1942 by Dr Harry Klinefelter and is one of the more common chromosomal conditions affecting males. An additional X chromosome is found in the cells of these affected boys, giving them two X chromosomes instead of the usual one (see later).
The condition affects between 1 in 500 and 1 in 1000 males born each year in Australia.
A syndrome is a condition distinguished by a number of features that often occur together. There are a number of features that can be present in XXY syndrome.
Some affected boys will have more features of the syndrome than others and there will be a difference in the degree of severity of the symptoms between affected boys. In some cases, a diagnosis of XXY syndrome is not made until a boy approaches puberty and some men may never be diagnosed with the condition.
Features include
In each human cell, except the egg and sperm cells, there are 46 chromosomes, made up of 23 pairs (see Genetics Fact Sheet 1). There are
When egg and sperm cells are formed, the chromosome pairs separate so that there is only one of each pair in these cells ie. 23 chromosomes instead of 46.
A baby is conceived when the egg from the mother and the sperm from the father come together. The baby would then have two copies of each chromosome (46 chromosomes in total) just like the parents.
One copy of each chromosome would have come from the mother and one copy from the father.
Sometimes, when the egg and sperm are forming, a mistake occurs so that the chromosome pairs do not separate in an ordered fashion. The result is an egg or sperm cell that has only 22 chromosomes while others have 24 chromosomes.
If an egg or sperm carrying 24 chromosomes combines with an egg or sperm carrying the usual 23 chromosomes, the result would be an individual with cells in which there are 47 chromosomes instead of the usual 46 (Figure 31.1).
Figure 31.1: When the egg has 24 chromosomes, and the sperm has the usual 23, the baby's cells will contain 47 chromosomes instead of 46. This may also happen in the reverse situation.
Thus there would be three copies of a particular chromosome in the cells rather than the usual two copies (see Genetics Fact Sheet 6).
In addition to 22 pairs of autosomes (chromosomes that are numbered 1-22), males usually have two sex chromosomes: one X chromosome copy that they receive from their mother and a Y chromosome copy that they receive from their father.
Every egg has an X chromosome and every sperm has either an X or a Y chromosome.
Figure 31.2: Chromosome picture (karyotype) from a male with XXY syndrome
(SEALS Genetics, Prince of Wales Hospital, Randwick)..
In some very rare cases, males may have three or four extra X chromosome copies: 48,XXXY or 49,XXXXY.
Those boys who have one of these less common chromosome arrangements will show more exaggerated features of XXY syndrome and intellectual disability may be present.
When a mistake in cell division affecting the sex chromosomes occurs soon after conception, the chromosomes in the cells of the boys may show two different patterns. This is called chromosomal mosaicism and means that some boys who have XXY syndrome have some of their body cells containing 47 chromosomes because of an extra copy of the X chromosome, while other cells in their body have the usual 46 chromosomes. The boy is said to be mosaic for XXY syndrome (see Genetics Fact Sheet 13).
XXY syndrome results from an error during the division of the sex chromosomes in either the egg or the sperm. Such an event is said to occur sporadically (spontaneously for unknown reasons) and it is highly unlikely to affect further children.
Having a son with XXY syndrome does not appear to be related to either the age of the mother or the father at the time of conception.
This is unlike other chromosomal conditions where there is an extra chromosome copy in the cells, eg. trisomy 21 (Down syndrome - see Genetics Fact Sheet 28), where the mother's age is a factor.
Men with 47,XXY in all their cells are highly unlikely to ever have children naturally. Advances in assisted reproductive technologies (ART), however, are assisting in overcoming their fertility problems.
Those who are mosaic for XXY syndrome and have some cells with the usual 46,XY complement may be able to father children unassisted. Therefore it may be possible for a man with 47,XXY to have a child who also has 47,XXY, but this has not been recorded to date.
There is no cure for XXY syndrome. There are, however, a number of treatments that are aimed at reducing the impact of the symptoms of the condition.
In XXY syndrome, the testes do not function normally so that the production of the male hormone called testosterone is reduced. This means that the bodily changes that occur at puberty are impacted. Treatment is with the administration of male hormones (androgens) that promote the development of the secondary sexual characteristics (virilisation). This treatment starts when the boy is around 11-12 years but does not restore function to the testes and infertility remains. The therapy continues until late adulthood.
The use of testosterone therapy has secondary benefits in helping to improve self-image and self-esteem. This in turn will impact on a boy's performance at school and his ability to form friendships. Learning problems and language deficits can be helped with expert intervention following a thorough assessment.
There are several prenatal screening and diagnostic tests that can be done during pregnancy to determine if the baby is at risk of having, or definitely has XXY syndrome.
In addition, preimplantation genetic diagnosis (PGD) allows for testing for XXY syndrome on an embryo that has been created using assisted reproductive technology (ART) such as in vitro fertilisation (IVF). If the embryo does not have the condition, it is transferred to the uterus and allowed to develop normally (see Genetics Fact Sheet 18).
Any consideration of testing before or during pregnancy should only be made on an informed basis following appropriate counselling (see Genetics Fact Sheet 3).
Other Genetics Fact Sheets referred to in this Fact Sheet: 1, 3, 6, 13, 17, 17B, 17C, 18, 28
Australian Institute of Health and Welfare. (2004). Australia's babies, their health and wellbeing. Bulletin Issue 21[online].Available from: www.aihw.gov.au/publications/aus/bulletin21. [Accessed June 2007]
Gardner RJM and Sutherland G.(2004). Chromosome abnormalities and genetic counselling. 3rd ed. New York: Oxford University Press
National Organisation for Rare Disorders (NORD) [online]. Available from: http://www.rarediseases.org/. [Accessed June 2007]
Read A and Donnai D. (2007). New clinical genetics. Bloxham, Oxfordshire: Scion Publishing Ltd
June 2007 (3rd Ed)
Author/s: A/Prof Kristine Barlow-Stewart
Acknowledgements this edition: Gayathri Parasivam
Previous editions: 2004, 2002
Acknowledgements previous editions: Mona Saleh; Bronwyn Butler; Stuart Purvis-Smith; Prof Graeme Morgan; Association of Genetic Support of Australasia