Difference between revisions of "Monosomy X"
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*Broad chest. | *Broad chest. | ||
*Ovarian dysgenesis. | *Ovarian dysgenesis. | ||
Lame memory device ''NO CBC'': | |||
*'''N'''uchal edema, '''O'''varian dysgenesis, '''C'''ystic hygroma, '''B'''road chest, '''C'''oarctation of the aorta. | |||
Images: | Images: | ||
*[http://commons.wikimedia.org/wiki/File:45,X.jpg Monoxomy X karyotype (WC)]. | *[http://commons.wikimedia.org/wiki/File:45,X.jpg Monoxomy X karyotype (WC)]. | ||
*[http://commons.wikimedia.org/wiki/File:Puffy_feet.JPG Lymphedema (WC)]. | *[http://commons.wikimedia.org/wiki/File:Puffy_feet.JPG Lymphedema (WC)]. | ||
==See also== | ==See also== | ||
Revision as of 05:04, 10 October 2011
Monosomy X, also known as Turner syndrome is a relatively common chromosomal abnormality.
Characteristics
Features:[1]
- Cystic hygroma.
- Nuchal edema.
- Coarctation of the aorta.
- Broad chest.
- Ovarian dysgenesis.
Lame memory device NO CBC:
- Nuchal edema, Ovarian dysgenesis, Cystic hygroma, Broad chest, Coarctation of the aorta.
Images:
See also
References
- ↑ Sherman, C. Recent advances in pathology (lecture). 9 May 2011.