ISBN: 9780199591473

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 characterized by loss of the ability… Mehr…

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 characterized by loss of the ability to walk around the age of 10 or 11, leading to a wheelchair life, and death from cardiac and respiratoryproblems 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 researchers know 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 inheritedcondition 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 ofMeryon''s research which has led to our current understanding of the disease, will full references 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. | The History of a Genetic Disease by Alan E. H. Emery Hardcover | Indigo Chapters Kids' & Toys > Health & Well Being > Medical P10178, Alan E. H. Emery<

2011, ISBN: 9780199591473

Duchenne Muscular Dystrophy or Meryon's Disease, Buch, Hardcover, 2nd Revised edition, Duchenne Muscular Dystrophy is a disease that only affects males, with an incidence of around 1 in 3… Mehr…

Duchenne Muscular Dystrophy or Meryon's Disease, Buch, Hardcover, 2nd Revised edition, 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 characterized by loss of the ability to walk by around the age of 10 or 11, leading to a wheelchair life, and death 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, with full references 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. [PU: Oxford University Press], Seiten: 256, Oxford University Press, 2011<