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The History of a Genetic Disease - Duchenne Muscular Dystrophy or Meryon's Disease (Hardcover, 2nd Revised edition)
Loot Price: R4,828
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The History of a Genetic Disease - Duchenne Muscular Dystrophy or Meryon's Disease (Hardcover, 2nd Revised edition)
Series: Oxford Medical Histories
Expected to ship within 12 - 17 working days
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Duchenne Muscular Dystrophy is a disease that only affects males,
with an incidence of around 1 in 3500 new-born baby boys. Its
relentless progress is charterized by loss of the ability to walk
by around the age of 10 or 11, leading to a wheelchair life, and
dealth from cardiac and respiratory problems usually around the
late teens or early twenties.
Edward Meryon was the first person to give a full and detailed
clinical description of what later research knows as Duchenne
Muscular Dystrophy. His research identified many facets of the
condition which we now take for granted, for example that it only
affects males, that it is an inherited condition carried in female
genes, that it is a disease of the muscle system, and its causes.
Until recently, Meryon has not been given credit for his
contribution to the subject. In this book, the history of Duchenne
Muscular Dystrophy is traced in detail, and is interwoven with a
commentary of Meryon's research which has led to our current
understanding of the disease, will full refences and informative,
historically relevant illustrations.
This book concludes with a summary of the current position
regarding diagnosis, prevention through counselling and prenatal
diagnosis, and new encouraging approaches to treatment through
molecular genetics.
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