XX male syndrome: Difference between revisions
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==Overview== | ==Overview== | ||
'''XX male syndrome''' (also called '''de la Chapelle syndrome''', for a researcher who characterized it in 1972<ref>{{cite journal | author=de la Chapelle A | title=Analytic review: nature and origin of males with XX sex chromosomes | journal=Am J Hum Genet | year=1972 | pages=71–105 | volume=24 | issue=1 | pmid=4622299}}</ref>) is a rare sex chromosomal disorder. Usually it is caused by unequal [[Chromosomal crossover|crossing over]] between [[X chromosome|X]] and [[Y chromosome]]s during [[meiosis]]. | '''XX male syndrome''' (also called '''de la Chapelle syndrome''', for a researcher who characterized it in 1972<ref>{{cite journal | author=de la Chapelle A | title=Analytic review: nature and origin of males with XX sex chromosomes | journal=Am J Hum Genet | year=1972 | pages=71–105 | volume=24 | issue=1 | pmid=4622299}}</ref>) is a rare sex chromosomal disorder. Usually it is caused by unequal [[Chromosomal crossover|crossing over]] between [[X chromosome|X]] and [[Y chromosome]]s during [[meiosis]]. | ||
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==References== | ==References== | ||
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[[Category:Genetic disorders]] | [[Category:Genetic disorders]] |
Latest revision as of 16:01, 6 September 2012
XX male syndrome | |
OMIM | 278850 |
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Overview
XX male syndrome (also called de la Chapelle syndrome, for a researcher who characterized it in 1972[1]) is a rare sex chromosomal disorder. Usually it is caused by unequal crossing over between X and Y chromosomes during meiosis.
It is less common than Klinefelter syndrome.[2]
Presentation
Symptoms include small testes, gynecomastia and sterility. Many individuals with this condition also have effeminate characteristics.
Pathophysiology
Men typically have one X chromosome and one Y chromosome in each diploid cell of their bodies. Women typically have two X chromosomes.
So-called XX males have two X chromosomes; thus they are genetically female but otherwise appear to be male.
See also
- Swyer syndrome
- X chromosome, for other diseases related to the X chromosome.
References
- ↑ de la Chapelle A (1972). "Analytic review: nature and origin of males with XX sex chromosomes". Am J Hum Genet. 24 (1): 71–105. PMID 4622299.
- ↑ Vorona E, Zitzmann M, Gromoll J, Schüring AN, Nieschlag E (2007). "Clinical, endocrinological, and epigenetic features of the 46,XX male syndrome, compared with 47,XXY Klinefelter patients". J. Clin. Endocrinol. Metab. 92 (9): 3458–65. doi:10.1210/jc.2007-0447. PMID 17579198. Unknown parameter
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