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Edwards Syndrome Research Paper

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What is Edwards syndrome
Edwards syndrome also known as trisomy 18 is a condition in which you have 3 chromosome 18 instead of your normal 2. A chromosome are thread like structures in the cells that hold genes. The genes carry everything need to create the baby's body. Many things go wrong when you have this condition, a few being miscarriage, low birth weight, small heads, under formed jaw, and malformed ears. Sadly this condition cannot be prevented nor is it inherited it effects random babies, we will be taking a look at all of these things.
How do you get Edwards syndrome
Edwards syndrome is started in the womb of the mother when the spem and egg meets and form the embryo, their chromosome combine. The baby gets 23 chromosomes from their …show more content…
Full trisomy 18: This is where the extra chromosome is in every cell of the baby's body, this is also the most common of the three.
Partial trisomy 18: The child in this case would only have part of an extra chromosome 18, that extra part could be attached to another chromosome in the egg or the sperm this is called a translocation. This type of trisomy is very rare.
Mosaic trisomy 18: The extra 18th chromosome is only found in some of the baby's cell, this type is also …show more content…
The most common being Low birth weight, chest deformities, small jaw and mouth, weak cry, overlapping fingers, and clenched fists, rocker bottom feet, low off set ears, esophagus doesn’t connect to the stomach, pocket of fluid in the brain, defects of the heart and other internal organs. Other signs that are less common are organs can be outside of the body when born, strawberry shaped head, umbilical hernia, poor feeding, respiratory problems, delayed growth, cleft palate lip, fingers and toes webbed together. In every case of Edwards syndrome the signs and symptoms will differ, it all depend on which trisomy you have and how your body handles

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