Muscular Dystrophy - Research Article from Encyclopedia of Childhood and Adolescence

This encyclopedia article consists of approximately 3 pages of information about Muscular Dystrophy.

Muscular Dystrophy - Research Article from Encyclopedia of Childhood and Adolescence

This encyclopedia article consists of approximately 3 pages of information about Muscular Dystrophy.
This section contains 868 words
(approx. 3 pages at 300 words per page)
Buy the Muscular Dystrophy Encyclopedia Article

A category of inherited, incurable, and often life-threatening diseases in which the limb and trunk muscles deteriorate.

The major types of muscular dystrophy (MD) are Duchenne, limb-girdle, facioscapulohumeral (FSH), Becker, and myotonic. In the United States, 250,000 people are affected by muscular dystrophy, with boys disproportionally represented at the rate of one in every 4,000 births.

Duchenne, the most severe form of muscular dystrophy, is passed exclusively by a defective gene in the mother to her son. A woman with the defective gene has a 50% chance of bearing a son with Duchenne muscular dystrophy. Female children of carrier mothers have a 50% chance of being carriers themselves. In this disease, the muscles of the lower body and spine are affected first; onset is in early childhood between the ages of two and six years. Nearly one-half of all Duchenne victims do not walk until after they reach 18 months old...

(read more)

This section contains 868 words
(approx. 3 pages at 300 words per page)
Buy the Muscular Dystrophy Encyclopedia Article
Copyrights
Gale
Muscular Dystrophy from Gale. ©2005-2006 Thomson Gale, a part of the Thomson Corporation. All rights reserved.