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Limb-girdle Muscular Dystrophy

Limb-girdle Muscular Dystrophy: Introduction

Limb-girdle Muscular Dystrophy: A condition which is characterized by a slowly progressive muscular dystrophy. More detailed information about the symptoms, causes, and treatments of Limb-girdle Muscular Dystrophy is available below.

Symptoms of Limb-girdle Muscular Dystrophy

Wrongly Diagnosed with Limb-girdle Muscular Dystrophy?

Limb-girdle Muscular Dystrophy: Related Patient Stories

Limb-girdle Muscular Dystrophy: Deaths

Read more about Deaths and Limb-girdle Muscular Dystrophy.

Limb-girdle Muscular Dystrophy: Complications

Review possible medical complications related to Limb-girdle Muscular Dystrophy:

Causes of Limb-girdle Muscular Dystrophy

Read more about causes of Limb-girdle Muscular Dystrophy.

Disease Topics Related To Limb-girdle Muscular Dystrophy

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

Misdiagnosis and Limb-girdle Muscular Dystrophy

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Limb-girdle Muscular Dystrophy: Research Doctors & Specialists

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Evidence Based Medicine Research for Limb-girdle Muscular Dystrophy

Medical research articles related to Limb-girdle Muscular Dystrophy include:

Click here to find more evidence-based articles on the TRIP Database

Limb-girdle Muscular Dystrophy: Animations

Research about Limb-girdle Muscular Dystrophy

Visit our research pages for current research about Limb-girdle Muscular Dystrophy treatments.

Clinical Trials for Limb-girdle 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 Limb-girdle Muscular Dystrophy include:

Statistics for Limb-girdle Muscular Dystrophy

Limb-girdle Muscular Dystrophy: Broader Related Topics

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Definitions of Limb-girdle Muscular Dystrophy:

A heterogenous group of inherited muscular dystrophy that can be autosomal dominant or autosomal recessive. There are many forms (called LGMDs) involving genes encoding muscle membrane proteins such as the sarcoglycan (SARCOGLYCANS) complex that interacts with DYSTROPHIN. The disease is characterized by progressing wasting and weakness of the proximal muscles of arms and legs around the HIPS and SHOULDERS (the pelvic and shoulder girdles). - (Source - Diseases Database)

An autosomal recessive form of muscular dystrophy that appears anywhere from late childhood to middle age; characterized by progressive muscular weakness beginning either in the shoulder or pelvic girdle; usually progresses slowly with cardiopulmonary complications in the later stages - (Source - WordNet 2.1)

Limb-girdle 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 Limb-girdle Muscular Dystrophy, or a subtype of Limb-girdle Muscular Dystrophy, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

 

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