Name: The History of a Genetic Disease: Duchenne Muscular Dystrophy or Meryon's Disease (Oxford Medical Histories) (en Inglés)
Price: 281180.00 CLP
Availability: InStock
Author: Alan E. H. Emery; Marcia L. H. Emery
ISBN: 9780199591473

portada The History of a Genetic Disease: Duchenne Muscular Dystrophy or Meryon's Disease (Oxford Medical Histories) (en Inglés)

The History of a Genetic Disease: Duchenne Muscular Dystrophy or Meryon's Disease (Oxford Medical Histories) (en Inglés)

Formato

Libro Físico

Editorial

Oxford University Press

Autor

Alan E. H. Emery; Marcia L. H. Emery

Año

2011

Idioma

Inglés

N° páginas

256

Encuadernación

Tapa Dura

Peso

1.30

ISBN13

9780199591473

N° edición

The History of a Genetic Disease: Duchenne Muscular Dystrophy or Meryon's Disease (Oxford Medical Histories) (en Inglés)

Alan E. H. Emery; Marcia L. H. Emery (Autor) · Oxford University Press · Tapa Dura

Libro Nuevo Importado

Envío: 11 a 15 días háb.

$ 562.350$ 281.180

-50%

Costos de importación incluídos en el precio ✅

Libro Nuevo

Quedan 10 unidades

$ 281.180

Llega entre el 06 Ago y el 12 Ago a Santiago, Región Metropolitana. Seleccionar ubicación

Agregar a lista de deseos

Reseña del libro "The History of a Genetic Disease: Duchenne Muscular Dystrophy or Meryon's Disease (Oxford Medical Histories) (en Inglés)"

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.