Difference between revisions of "Chromosomal anomalies"
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The most common ones in live born infants are:<ref>{{Ref PCPBoD8|237}}</ref> | The most common ones in live born infants are:<ref>{{Ref PCPBoD8|237}}</ref> | ||
*Trisomy 21 (Down syndrome). | *[[Trisomy 21]] (Down syndrome). | ||
*Klinefelter syndrome (47 XXY). | *[[Klinefelter syndrome]] (47 XXY). | ||
*Monosomy X (45 X, AKA Turner syndrome). | *[[Monosomy X]] (45 X, AKA Turner syndrome). | ||
*Trisomy 13 (Patau syndrome). | *[[Trisomy 13]] (Patau syndrome). | ||
*Trisomy 18 (Edwards syndrome). | *[[Trisomy 18]] (Edwards syndrome). | ||
==References== | ==References== | ||
Revision as of 13:20, 16 May 2011
Chromosomal anomalies are common enough in paediatrics that one ought to know about 'em.
The most common ones in live born infants are:[1]
- Trisomy 21 (Down syndrome).
- Klinefelter syndrome (47 XXY).
- Monosomy X (45 X, AKA Turner syndrome).
- Trisomy 13 (Patau syndrome).
- Trisomy 18 (Edwards syndrome).
References
- ↑ Mitchell, Richard; Kumar, Vinay; Fausto, Nelson; Abbas, Abul K.; Aster, Jon (2011). Pocket Companion to Robbins & Cotran Pathologic Basis of Disease (8th ed.). Elsevier Saunders. pp. 237. ISBN 978-1416054542.