Turner

Turner syndrome: A Congenital Anomaly
Our genes play an important fictional character in how we look, what diseases we are at risk for and it
even sets the grade for what our children will inherit. In 1928, a physician, named Henry H.
Turner prototypical identified the characteristics of what today is known as Turner Syndrome. In 1959,
another physician named Dr. Ford discovered a behavior to diagnose Turner syndrome through
chromosomal analysis. This allowed physicians to identify Turner Syndrome great before the
child showed any characteristics of the syndrome (Scheuerle, 2005). Turner syndrome is defined
as a chromosomal disorder, which affects females and causes abnormal sexual development.
According to the statistics Turner syndrome exists in 1 out of every 2,500 live female
births. Amazing this barely accounts for 2% of pregnancies. (U.S. Depa r tmen t of , 2010) .
When the newly deve loped ovum i s c r e a t ed e a ch pa r ent spend a penny s 23
chromos ome s c r e a t ing a tot a l of 46 chromos ome s . The gende r of the chi ld
to be i s de t e rmin ed b y a comb ina t ion of XX, which makes it a girl or XY, which
makes it a boy (Trewinnard, 2005). In Turner syndrome the X chromosome is damaged or
missing.



If wizard(a) of the parent pass a damaged X chromosome a spontaneous abortion will most
likely occur still in most cases if the male parent passes the damaged X chromosome or rather
does not pass the X chromosome, the pregnancy may have a chance to survive with only one X
chromosome, which was received by the mother. Once the ovum develops the first 10 weeks
will be the most important in find the development that will occur. After those ten weeks
the fetus endurance rate increases (Scheuerle, 2005). However, the National Human
Genome Re s e a r ch Ins t i tut e c a l l s i t a random error that happens during the forma t ion of the egg or s pe rm thus s t a t ing tha t f ami l i e s do not inhe r i t thi s
s yndrome (Na t iona l Human Genome , 2008) .
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