Jump to content

Edwards syndrome

From Simple English Wikipedia, the free encyclopedia

Trisomy 18, also known as Edwards syndrome is a trisomy. It is a genetic disorder. People with trisomy 18 have three copies of chromosome 18. "Normal" people have two copies of the chromosome. It is named after John H. Edwards, who first described the syndrome in 1960.[1] It is the second most common autosomal trisomy, after Down Syndrome, that carries to term.

It is estimated that about one in 3,000 live births are affected.[2] The incidence increases as the mother's age increases. The syndrome has a very low rate of survival. People with Edwards syndrome often have heart abnormalities, kidney malformations, and other internal organ disorders.

About 95% of the babies with Edwards syndrome die before they are born. About half of all babies born with the condition will reach two months of age, and only 5-10% will survive for a year. The median life span is five to fifteen days.[3][4] One percent of children born with this syndrome live to age ten, typically in cases of the less severe mosaic Edwards syndrome.[5]

References[change | change source]

  1. "Edwards syndrome (John Hilton Edwards)". WhoNamedIt.com. Retrieved 2008-07-24.
  2. (2007, July 07). MedlinePlus medical encyclopedia: Trisomy 18. Retrieved November 7, 2008, from MedlinePlus medical encyclopedia Web site: https://www.nlm.nih.gov/MEDLINEPLUS/ency/article/001661.htm#Causes,%20incidence,%20and%20risk%20factors
  3. Rodeck, Charles H.; Whittle, Martin J. (1999). Fetal Medicine: Basic Science and Clinical Practice. Elsevier Health Sciences. ISBN 044305357X.[permanent dead link]
  4. Zoler, Mitchel L. (March 1, 2003). "Trisomy 13 survival can exceed 1 year". OB/GYN News. Archived from the original on 2012-07-18. Retrieved 2008-07-24.
  5. Chen, MD, Harold. "Introduction to Trisomy 18". EMedicine. Retrieved 2008-07-24.