Muscular Dystrophy

Muscular Dystrophy

Muscular dystrophy is a group of genetic disorders characterized by progressive muscle weakness and degeneration. It affects the muscles responsible for movement, leading to difficulties in mobility and muscle function. With various types and levels of severity, muscular dystrophy can have a significant impact on an individual’s quality of life. In this article, we will explore the causes, types, symptoms, and available treatment options for muscular dystrophy, providing a comprehensive understanding of this complex condition.

Causes:

Muscular dystrophy is primarily caused by genetic mutations that interfere with the production of proteins needed for healthy muscle function. These mutations can be inherited or occur spontaneously. The specific gene mutations involved determine the type of muscular dystrophy and its pattern of inheritance.

Symptoms:

While the symptoms of muscular dystrophy vary depending on the specific type, some common signs and symptoms include:
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