Noah
Meine
Mr.
Youell
9B
Science
October
10, 2014
Trisomy 13:
Patau Syndrome
In a recent article, published by Life Site a women
named Kara McHenry was informed on September 12th 2013 that she is
pregnant with a baby that had a genetic disorder called Trisomy 13, or commonly
referred to as the Patau Syndrome. Doctors told Kara and her husband, Shane, that having Trisomy 13 made baby Corbin “incompatible with life”, and that
there was a mere 1% chance that Corbin would be born breathing. No matter how
slim the odds were Kara wanted to keep the baby alive.
Baby Corbin
was born seven weeks premature and faced a very low chance of surviving. For
most babies with Trisomy 13, there is a 5-10% chance of surviving the first few
days. For Corbin this chance was less than 1%. However, despite the odds present, Corbin survived the first few days and continued fighting on. From then on Kara began celebrating Corbin’s
life through a Facebook page named “Prayers for Corbin”. Kara would post a
picture of Corbin every day and receive support from strangers. Corbin passed
away at 135 days and had gained over half a million fans on Facebook. His
parents and fans mourned his death, but at the same time celebrated his life.
Below you can see Corbin at 115 days old (Figure 1).
Figure 1: Bay Corbin at 115 Days Old |
So what is Trisomy 13, and how did
it affect Corbin genetically? Trisomy 13 or Patau syndrome is a genetic
disorder. The term trisomy is used to describe the presence of three
chromosomes, rather than the usual pair of chromosomes. In Trisomy 13 there are
three copies of genetic material from chromosome 13, instead of the typical
two copies, or pair of chromosomes. Trisomy 13 occurs when there is extra DNA
is present in some or all of the body cells, and it is caused by nondisjunction
during meiosis. As far as scientists know Trisomy 13 cannot be inherited,
however according to The University
of Rochester Medical Center the chance of
a baby being born with Trisomy 13 increases as the mother ages. Trisomy 13 also includes a number of birth
defects. This includes intellectual disability, as well as physical
problems involving nearly every organ system in the body. Lastly Trisomy 13
occurs in approximately 1 out of every 1600 newborns.
In
conclusion, the significance of this story is more than a baby getting
attention for having a genetic mutation, but it is more about the fight for
survival and Trisomy 13 itself. This is also significant to people suffering
from any chromosomal disorder and how science can help us predict genetic disorders
and how people will still care about each other regardless.
Interesting story and Patau Syndrome was well explained. Your whole body of work was a nice length and it kept me interested the whole time I was reading.
ReplyDeleteGreat story, good source. You chose a good picture but you could also have a picture of the karyotype. Even though, I had the same syndrome for my project, and I have read many articles about it, reading your story was really interesting. I like how you mention how science can help us make the life of those people better. Your explanation about the disorder is also good and easily understood.
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