Trisomy 18 (cont.)
Melissa Conrad Stöppler, MD
Melissa Conrad Stöppler, MD, is a U.S. board-certified Anatomic Pathologist with subspecialty training in the fields of Experimental and Molecular Pathology. Dr. Stöppler's educational background includes a BA with Highest Distinction from the University of Virginia and an MD from the University of North Carolina. She completed residency training in Anatomic Pathology at Georgetown University followed by subspecialty fellowship training in molecular diagnostics and experimental pathology.
David Perlstein, MD, MBA, FAAP
Dr. Perlstein received his Medical Degree from the University of Cincinnati and then completed his internship and residency in pediatrics at The New York Hospital, Cornell medical Center in New York City. After serving an additional year as Chief Pediatric Resident, he worked as a private practitioner and then was appointed Director of Ambulatory Pediatrics at St. Barnabas Hospital in the Bronx.
In this Article
- Trisomy 18 facts
- What is trisomy 18?
- What are the chromosome basics of trisomy 18?
- What are the characteristic signs and symptoms of trisomy 18?
- How common is trisomy 18?
- How is trisomy 18 diagnosed?
- Can people with trisomy 18 survive to adulthood?
- Is there any treatment for trisomy 18?
- Find a local Doctor in your town
What is trisomy 18?
Trisomy 18, also known as Edwards Syndrome, is a severe genetic disorder associated with intellectual disability and abnormalities in many organs. Trisomy 18 was first described in 1960 and results from an additional copy of chromosome 18 (normal cells carry two copies of each chromosome; the term, "trisomy," refers to the presence of three of a given chromosome). Only about 10% of affected infants survive past one year of age, and half of affected infants do not live beyond the first week of life.
What are the chromosome basics of trisomy 18?
In most cases of trisomy 18, all the cells in the body have an extra copy of chromosome 18. Around 5% of affected people have the extra chromosome 18 in some, but not all, of the body's cells. This phenomenon is known as mosaic trisomy 18. Mosaic trisomy 18 may be very severe or hardly noticeable, depending upon the number of cells that have the extra chromosome.
In rare cases, there is no extra chromosome present; rather, a portion of the long arm of chromosome 18 becomes attached to another chromosome during the formation of egg and sperm cells or very early in development of the embryo. In this case, the individual has two copies of chromosome 18 plus the additional material from chromosome 18 that is attached to another chromosome. This is known as translocation, and the extra genetic material causes the developmental abnormalities in the same way as the presence of an entire extra chromosome. The signs and symptoms of this form of trisomy 18 are dependent upon the amount of chromosomal material that was translocated to another chromosome.
Trisomy 18 is not an inherited condition; it occurs as the result of random events during egg and sperm formation. The type of error that occurs is known as nondisjunction, and this leads to an egg or sperm cell with an abnormal number of chromosomes.
It is not known precisely why the extra genetic material causes the abnormalities specific to trisomy 18. As with Down syndrome (trisomy 21), experts believe that the presence of the extra chromosomal material interferes with the expression and interaction of various genes, resulting in impaired development and function.
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