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Diagnosis of Turner syndrome Name Institution Turner syndrome is a chromosome abnormality condition named after Henry Turner, endocrinologist , where the females lack or abnormalities in the part or entire sex chromosome, scientifically called monosomy x (Tohem, Tsuang & Goodwin, 2006).
The condition has various symptoms, some of which are physical while the rest are biological (American Psychiatric Association, 2004). Physical symptoms include swollen broad necks, webbed necks, and reduced hair line, hanging ears and swollen eyes among others. Biological symptoms are irregular or no menstrual cycle. The condition could further to certain complications like heart diseases, impaired vision and hearing, diabetes and thyroid complications among others. This discourse is about turner syndrome, explaining its causes, symptoms and diagnosis among other relevant subjects. Causes Turner syndrome arises from absence or abnormalities of the x chromosomes in part or whole of the cells. A normal girl should have two x chromosomes inherited from both the male and female parents (Bondy, 2009). However, one of the x chromosomes may be affected or missing in the sex cells rising to turner syndrome. Abnormalities of the x chromosomes could rise from mosaicism, a condition resulting from inappropriate cell division in the early days or stages of fetal developments (Bondy, 2009). This may cause variations in the cells composition, with some having two x chromosomes while others having only one X chromosome (Bondy, 2009). Furthermore, a cell may have both complete and faulty X chromosome. ...
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