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Muscular Dystrophy Types: Symptoms, Causes, Treatment: Publications and Documents

Summary

The Disabled World list of information on Muscular Dystrophy Types provides a broad overview of various forms of this condition, covering topics such as Duchenne, Becker, limb-girdle, and congenital muscular dystrophies, along with discussions on symptoms, diagnosis, and potential management approaches. This collection includes articles and general information pieces intended to be accessible and informative for a wide audience, including individuals with disabilities, seniors, and their families, offering insights into understanding different types of muscular dystrophy and related challenges. The publications offer valuable insights into symptoms, genetic causes, progression, and potential treatments for each type. This information can be particularly beneficial for individuals with disabilities, seniors, and their caregivers, as it helps them better understand the condition and make informed decisions about care and management. The articles are written in an accessible style, making complex medical information more understandable for a general audience while still maintaining scientific accuracy.

Searching the Database

The data table below lists items that may have been updated or revised, but the table defaults to sorting by descending publication date; you can search and sort by clicking column headers (JavaScript required). Items in this category are also distributed via our Muscular Dystrophy Types: Symptoms, Causes, Treatment RSS feed.

Muscular Dystrophy Types: Symptoms, Causes, Treatment: Publications and Resources (15 Items)
Title and DescriptionEdPublish
Revised

A rare neuromuscular disorder diagnosis of Facioscapulohumeral Muscular Dystrophy (FSHD) brings long awaited answers for teenager.


U.S. Food and Drug Administration approves Exondys 51 (eteplirsen) injection to treat patients with Duchenne muscular dystrophy (DMD).

People with muscular dystrophy have to take the least amount of steroid that will give them the maximum therapeutic effect.

Cyclic bursts of a STAT3 inhibitor can replenish muscle stem cells and promote differentiation into muscle fibers. Findings are important step in developing and maintaining new muscle to treat muscle diseases.


In DMD the combination of the lack of dystrophin and inflammatory reactions causes the muscles to weaken and waste over time.

Successful Duchenne muscular dystrophy treatments would likely need to target muscle stem cells not just muscle fibers.

Advance in determining the cause of a common form of muscular dystrophy known as facioscapulohumeral dystrophy.

Rochester leads international effort to improve muscular dystrophy treatment.


Walker-Warburg Syndrome (WWS) is a rare genetic and multi-system disorder characterized by eye and brain abnormalities and muscle disease.


The first identification of a new form of adult onset muscular dystrophy.

Myotonic Dystrophy is a progressive disease involving muscle weakness in which the muscles are slow to relax after contracting.


Limb-Girdle Muscular Dystrophy includes a group of diverse disorders which affect voluntary muscles predominantly around the pelvic and shoulder areas.


Congenital Muscular Dystrophy is a group of diseases of the muscles. Understanding and technology related to these diseases are progressing.


Beckers Muscular Dystrophy is a form of inherited disorder characterized by progressive muscle weakness in the pelvis and legs.


Duchenne Muscular Dystrophy is a genetic degenerative diseases primarily affecting voluntary muscles and causing pain.

Key: the first check mark indicates the publication carries an editor's note; the second indicates a footnote.

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Database of <a href="https://www.disabled-world.com/disability/types/mobility/md-2/">Muscular Dystrophy Types: Symptoms, Causes, Treatment documents, papers, and peer reviewed publications</a> - Disabled World (DW).

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