
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.
This book investigates the historical evolution of Down syndrome, tracing its transformation from a misunderstood medical curiosity to a recognized genetic condition. David Wright, a Professor in the History of Medicine, utilizes archival medical records, historical literature, and social policy documentation to construct a comprehensive narrative. He argues that the history of the condition is as much a reflection of changing societal attitudes toward disability as it is a chronicle of clinical discovery.
What You Will Find
Scope Limits
Experts in the history of medicine recognize this work as a foundational text for understanding the intersection of genetics and social policy. Readers frequently note the academic rigor of the prose and the author's ability to contextualize medical terminology within broader cultural shifts.
Page Count:
254
Publication Date:
2011-01-01
Publisher:
OUP Oxford
ISBN-10:
0191619787
ISBN-13:
9780191619786
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