For 150 years, Down's Syndrome has constituted the archetypal mental
disability, easily recognisable by distinct facial anomalies and
physical stigmata. In a narrow medical sense, Down's syndrome is a
common disorder caused by the presence of all or part of an extra 21st
chromosome. It is named after John Langdon Down, the British asylum
medical superintendent who described the syndrome as Mongolism in a
series of lectures in 1866. In 1959, the disorder was identified as a
chromosome 21 trisomy by the French paediatrician and geneticist Jérôme
Lejeune and has since been known as Down's Syndrome (in the
English-speaking world) or Trisomy 21 (in many European countries). But
children and adults born with this chromosomal abnormality have an
important collective history beyond their evident importance to the
history of medical science.
David Wright, a Professor in the History of Medicine at McMaster
University, looks at the care and treatment of Down's sufferers -
described for much of history as 'idiots', - from Medieval Europe to the
present day. The discovery of the genetic basis of the condition and the
profound changes in attitudes, care, and early identification of Down's
in the genetic era, reflects the fascinating medical and social history
of the disorder.