Edward syndrome, also known as Trisomy 18, is a chromosomal condition caused by the presence of an extra copy of chromosome 18. It is associated with abnormalities in many parts of the body and was first described by John H. Edwards in 1960. Affected individuals often have physical characteristics like low birth weight, small head size, malformed ears and heart defects. Treatment focuses on palliative care as the condition is often fatal, with the majority of children passing away within their first year. Those who survive longer experience severe developmental delays.