Trisomy 22: Difference between revisions
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* {{cite journal |author=Mokate T, Leask K, Mehta S, ''et al'' |title=Non-mosaic trisomy 22: a report of 2 cases |journal=Prenat. Diagn. |volume=26 |issue=10 |pages=962–5 |year=2006 |pmid=16906599 |doi=10.1002/pd.1537}} | * {{cite journal |author=Mokate T, Leask K, Mehta S, ''et al'' |title=Non-mosaic trisomy 22: a report of 2 cases |journal=Prenat. Diagn. |volume=26 |issue=10 |pages=962–5 |year=2006 |pmid=16906599 |doi=10.1002/pd.1537}} | ||
{{Chromosomal abnormalities}} | {{Chromosomal abnormalities}} | ||
[[de:Trisomie 22]] | [[de:Trisomie 22]] | ||
Revision as of 17:07, 20 August 2012
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Trisomy 22 is a chromosomal disorder in which there are three copies of chromosome 22 rather than two. It is a frequent cause of spontaneous abortion during the first trimester of pregnancy. Progression to the second trimester and livebirth are rare.
References
- Mokate T, Leask K, Mehta S; et al. (2006). "Non-mosaic trisomy 22: a report of 2 cases". Prenat. Diagn. 26 (10): 962–5. doi:10.1002/pd.1537. PMID 16906599.
Template:Chromosomal abnormalities
de:Trisomie 22
he:טריזומיה 22
nl:Trisomie 22