Difference between revisions of "Chromosomal anomalies"
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==References== | ==References== | ||
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[[Category:Pediatric pathology]] | [[Category:Pediatric pathology]] | ||
Revision as of 03:33, 13 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.