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Diseases » Duchenne Muscular Dystrophy » Introduction
 

Duchenne Muscular Dystrophy

Duchenne Muscular Dystrophy: Introduction

A genetic recessive disease that affects muscles causing progressive and degenerative muscle weakness. It is caused by a mutation in the dystrophin gene that creates a protein that anchors muscle fibers in cells.

Symptoms of Duchenne Muscular Dystrophy

See full list of 25 symptoms of Duchenne Muscular Dystrophy

Duchenne Muscular Dystrophy: Complications

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Disease Topics Related To Duchenne Muscular Dystrophy

Research the causes of these diseases that are similar to, or related to, Duchenne Muscular Dystrophy:

Medical Textbooks Online about Duchenne Muscular Dystrophy

Medical Books Excerpts
 

Book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.

Diagnostic Tests for Duchenne Muscular Dystrophy

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Wrongly Diagnosed with Duchenne Muscular Dystrophy?

Misdiagnosis and Duchenne Muscular Dystrophy

Delay in onset of walking may be Duchenne's: Duchenne Muscular dystrophy affects the proximal muscles causing weakness. It is an X- linked recessive disorder. The child usually presents with delay in walking, frequent falls and standing difficulty. Becker's Muscular Dystrophy is a disease with similar aspect and distribution to the Duchenne Muscular Dystrophy, although it is usually less severe. No specific treatment is available although steroids delay the progression of the disease. Most patients die of respiratory problems by the age of 20. Maternal screening must be done....read more »

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Causes of Duchenne Muscular Dystrophy

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Treatments for Duchenne Muscular Dystrophy

Read more about treatments for Duchenne Muscular Dystrophy

News Archives for Duchenne Muscular Dystrophy

Medical news articles related to Duchenne Muscular Dystrophy include:

Source: HealthDay News

Evidence Based Medicine Research for Duchenne Muscular Dystrophy

Medical research articles related to Duchenne Muscular Dystrophy include:

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Patient Surveys for Duchenne Muscular Dystrophy

Reseach about Duchenne Muscular Dystrophy

Visit our research pages for current research about Duchenne Muscular Dystrophy treatments.

Clinical Trials for Duchenne Muscular Dystrophy

The US based website ClinicalTrials.gov lists information on both federally and privately supported clinical trials using human volunteers.

Some of the clinical trials listed on ClinicalTrials.gov for Duchenne Muscular Dystrophy include:

See full list of 16 Clinical Trials for Duchenne Muscular Dystrophy

Statistics for Duchenne Muscular Dystrophy

Duchenne Muscular Dystrophy: Broader Related Topics

Types of Duchenne Muscular Dystrophy

Types of Duchenne Muscular Dystrophy

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Stories from Users Related to Duchenne Muscular Dystrophy

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Article Excerpts about Duchenne Muscular Dystrophy

Duchenne muscular dystrophy (DMD) is one of a group of muscular dystrophies characterized by the enlargement of muscles. DMD is one of the most prevalent types of muscular dystrophy and is characterized by rapid progression of muscle degeneration that occurs early in life. (Source: Genes and Disease by the National Center for Biotechnology)

Definitions of Duchenne Muscular Dystrophy:

An X-linked recessive muscle disease caused by an inability to synthesize DYSTROPHIN, which is involved with maintaining the integrity of the sarcolemma. Muscle fibers undergo a process that features degeneration and regeneration. Clinical manifestations include proximal weakness in the first few years of life, pseudohypertrophy, cardiomyopathy (see MYOCARDIAL DISEASES), and an increased incidence of impaired mentation. Becker muscular dystrophy is a closely related condition featuring a later onset of disease (usually adolescence) and a slowly progressive course. (Adams et al., Principles of Neurology, 6th ed, p1415) - (Source - Diseases Database)

Duchenne Muscular Dystrophy is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Duchenne Muscular Dystrophy, or a subtype of Duchenne Muscular Dystrophy, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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