What is muscular dystrophy? Learn the signs of muscular dystrophy, what causes it, how doctors diagnose it, and how to treat it. Read more: How Long Can you Live With Muscular Dystrophy? Article
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Brain Food Pictures: What to Eat to Boost Focus See SlideshowRelated Disease Conditions
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Reflex Sympathetic Dystrophy (RSD, Complex Regional Pain Syndrome Type 1, CRPS)
Reflex sympathetic dystrophy syndrome (RSD) is a condition that features atypical symptoms including pain (often "burning" type), tenderness, and swelling of an extremity associated with varying degrees of sweating, warmth and/or coolness, flushing, discoloration, and shiny skin. RSD is also referred to as "the shoulder-hand syndrome." Treatment response is greater in earlier stages than later stages.
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Neuropathic Pain
Neuropathic pain is a chronic condition that leads to ongoing pain symptoms. Patients can be predisposed to developing neuropathic pain who have conditions such as diabetes, cancer, stroke, HIV, vitamin deficiencies, shingles, and multiple sclerosis. Patient history and nerve testing are used to diagnose neuropathic pain. Antidepressants, antiseizure medications, and other types of medications are used to treat neuropathic pain. Many people with neuropathic pain are able to attain some level of relief.
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What Are the Symptoms of Myopathy?
The most common symptoms of myopathy are weakness and impaired daily functions or activities, as well as muscle pain and tenderness. General signs and symptoms of myopathy include symmetric proximal muscle weakness, fatigue and malaise, motor delay, bulbar muscle dystrophy (dysfunction of the swallowing and speech muscles), myoglobinuria (dark-colored urine) and/or fever, no paresthesia (sensory impairments), atrophy and hyporeflexia, consciousness at normal levels, and Gottron papules (dermatomyositis) over the knuckles, elbows, and knees.
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What Is an X Mutation?
X-linked refers to any ailment that has an X chromosomal connection. Mammals normally have two copies of the X chromosome in females and one in males, which is referred to as a sex chromosome. Compared to the Y chromosome, which has only about 70 protein-coding genes, the X chromosome in humans contains about 800 protein-coding genes. The genes located in the X chromosome are referred to as X-linked genes.
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What Is the Best Treatment for Muscular Dystrophy?
Learn what medical treatments can help with your muscular dystrophy symptoms and speed up your recovery.
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How Many Types of Muscular Dystrophy Are There?
Muscular dystrophy is a genetic disease that weakens and wastes away skeletal muscle. There are 30 different types of muscular dystrophy that fall into nine major categories. Learn what the symptoms of muscular dystrophy are, how you get muscular dystrophy, and what treatments there are for muscular dystrophy.
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What Is Muscular Dystrophy?
There are more than 30 types of muscular dystrophy that cause progressive muscle weakness, including Duchenne Becker (DMD), Becker (BMD), and more. Muscular dystrophy symptoms also include scoliosis (sideways curved spine), difficulty in walking or running, dysphagia (difficulty swallowing), muscle pain, breathing problems, and others.
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Muscular Dystrophy Types & Causes of Each Form
Muscular dystrophies are a group of genetic diseases causing progressive weakness and loss of muscle mass. There are more than 30 types of muscular dystrophy that result in muscle weakness. Over time, the muscles get weaker, disturbing the gait (a person’s manner of walking) and the ability to perform daily activities.
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