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Edwards' Syndrome

 
Medical Encyclopedia: Edwards' Syndrome

Definition

Edwards' syndrome is caused by an extra copy of chromosome 18. For this reason, it is also called trisomy 18 syndrome. The extra chromosome is lethal for most babies born with this condition. It causes major physical abnormalities and severe mental retardation, and very few children afflicted with this disease survive beyond a year.

Description

Humans normally have 23 pairs of chromosomes. Chromosomes are numbered 1–22, and the 23rd pair is composed of the sex chromosomes, X and Y. A person inherits one set of 23 chromosomes from each parent. Occasionally, a genetic error occurs during egg or sperm cell formation. A child conceived with such an egg or sperm cell may inherit an incorrect number of chromosomes.

In the case of Edwards' syndrome, the child inherits three, rather than two, copies of chromosome 18. Trisomy 18 occurs in approximately one in every 3, 000 newborns and affects girls more often than boys. Women older than their early thirties have a greater risk of conceiving a child with trisomy 18, but it can occur in younger women.

— Julia Barrett



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Sci-Tech Dictionary: trisomy 18 syndrome
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(′trī′sō·mē ′ā¦tēn ′sin′drōm)

(medicine) A congenital disorder due to trisomy of all or a large part of chromosome 18, characterized by severe mental deficiency, hypertonicity with clenched hands, and anomalies of the hands, sternum, pelvis, and facies; most infants so afflicted fail to thrive. Also known as Edwards' syndrome; E trisomy.


 
 

 

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