2011 Group Project 3

From Embryology
Revision as of 05:35, 18 August 2011 by Z3289991 (talk | contribs)
Note - This page is an undergraduate science embryology student group project 2011.
2011 Projects: Turner Syndrome | DiGeorge Syndrome | Klinefelter's Syndrome | Huntington's Disease | Fragile X Syndrome | Tetralogy of Fallot | Angelman Syndrome | Friedreich's Ataxia | Williams-Beuren Syndrome | Duchenne Muscular Dystrolphy | Cleft Palate and Lip

Kleinfelter Syndrome


Klinefelter's syndrome is a condition wherein a male has an extra X chromosome. Typically, men and women have two sex chromosomes, women have two X chromosomes (46,XX), while men have an X and Y chromosome (46,XY). '46' refers to the total number of chromosomes present including both autosomes and sex chromosomes. However, men with Klinefelter's syndrome have three sex chromosomes (47,XXY) due to a process known as non-disjunction[1].

In some very rare cases there are two or more extra copies of the X chromosome present (48,XXXY, or 49,XXXXY). This generally results in more prominent clinical features. In approximately 20% of cases, 46,XY/47,XXY mosaicism can occur[2]. This refers to the situation where the extra chromosome is only present in some cells, this is due to errors occurring during mitosis.

Klinefelter's syndrome usually presents with a few standard clinical abnormalities. Affected men can have reduced fertility and hypogonadism. However, a high proportion of affected men may not show any symptoms and the severity of the disorder differs greatly from person to person. It is thought to be one of the most common conditions caused by non-disjunction[3].

This disorder was first described by Harry F. Klinefelter in 1942 [4]. He describes a disorder characterised by gynecomastia and a very specific type of hypogonadism, as well as an absence of spermatogenesis.



The most common disorder of sex chromosomes in humans is 47, XXY mutations in around 1 in 500 males (Jr, 2006). There are variations of the Klinefelter syndrome chromosomal aneuploidies, with a frequency of 1 in 50 000 male births (Communications, 2008). Males born with Klinefelter syndrome tend to exhibit failure to produce sperm, and have low testosterone levels due to having very small testes. They have increased susceptibility to diabetes, cardiovascular disease and cancer (Kobayashi, 2011). In about 80% of all cases, Klinefelter’s syndrome is in every cell of the body. As well, having a child with Klinefelter’s syndrome is not relevant to the age of the mother or father at the time of conception (Barlow-Stewart, 2007). Usually, the phenotype of Klinefelter’s syndrome only becomes evident after puberty. Prior to puberty however, the pituitary gland and gonad function is relatively normal in sufferers of the condition (Wikström, 2011).

Signs and Symptoms




Androgen Therapy

Androgen therapy involves the replacement of testosterone. This is primarily given to stimulate the onset of puberty in affected males. Ideally, testosterone is given from the age that puberty usually occurs, in order to encourage normal development. In addition to this, it assists in treating or preventing some of the more typical clinical presentations of this disorder. Testosterone replacement encourages secondary sexual attributes, and helps ensure standard bone and muscle mass[5].

However, this has been assocciated with a decrease in fertility, especially if given early in life. Premature treatment has been suggested to result in delayed puberty and abnormal physical development during this period[6]. It is also recommended to stop testosterone replacement a few months prior to the administration of infertility treatment[7].


Aromatase inhibitors can be administered to men, in order to lower intrtesticular estradiol levels. This is thought to encourage the production of testosterone and activate spermatogenesis[8]. There are two main methods used to treat non-obstructive azoospermia, microdissection testicular sperm extraction (TESE) and conventional TESE. These are methods of extracting what sperm is present in the testes for use in in vitro fertilisation (IVF). It has been shown that microdissection TESE has a higher rate of extraction, and allows for minial testicular damage[9], and so conventional TESE is slowly being replaced by microdissection TESE. The most common IVF technique used in these situations is intracytoplasmic sperm injection, where a single sperm is injected into a single oocyte. This means that for the highest chance of success, the extraction of both the sperm and the egg need to be well timed[10]. Before surgery, men are usually administered aromatase inhibitors for a few months. This is to restore the ratio of testoserone to esradiol back to normal levels, and to encourage the amount of viable sperm present[11][12]

Other Similar Defects

Current Research



  1. <pubmed>17062147</pubmed>
  2. <pubmed>21397196</pubmed>
  3. <pubmed>17062147</pubmed>
  4. Klinefelter HF, Reifenstein EC & Albright F. Syndrome characterized by gynecomastia, aspermatogenesis without a-Leydigism, and increased excretion of follicle-stimulating hormone. American Journal of Clinical Dermatology 1942; 2: 615–627.
  5. <pubmed>20482304</pubmed>
  6. <pubmed>18832949</pubmed>
  7. <pubmed>18832949</pubmed>
  8. <pubmed>11792932</pubmed>
  9. <pubmed>21811543</pubmed>
  10. <pubmed>21716935</pubmed>
  11. <pubmed>11792932</pubmed>
  12. <pubmed>19616796</pubmed>

Barlow-Stewart, A. K. (2007). KLINEFELTER SYNDROME – XXY SYNDROME. Produced by the Centre for Genetics Education. Communications, L. H. (2008, July). Klinefelter Syndrome. Retrieved August 17, 2011, from Genetics Home Reference: http://ghr.nlm.nih.gov/condition=klinefelter-syndrome Kobayashi, H. (2011). Pluripotent Stem Cells Induced from Testicular Tissue of a Man with Klinefelter Syndrome (47, XXY) by Four Transcription Factors (OCT4, SOX2, KLF4, and C-MYC). Department of Urology, Toho University School of Medicine Japan, 295-306. Wikström, A. M. (2011). Klinefelter syndrome. Best Practice & Research Clinical Endocrinology & Metabolism, 239-250.

2011 Projects: Turner Syndrome | DiGeorge Syndrome | Klinefelter's Syndrome | Huntington's Disease | Fragile X Syndrome | Tetralogy of Fallot | Angelman Syndrome | Friedreich's Ataxia | Williams-Beuren Syndrome | Duchenne Muscular Dystrolphy | Cleft Palate and Lip