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Miyoshi myopathy

Miyoshi myopathy: Introduction

Miyoshi myopathy: A rare genetic condition characterized by slow-progressing muscle weakness and atrophy that starts in the calves and progresses to the rest of the legs and arms. Occasionally the hips and shoulders may be affected but the heart and facial muscles are spared. More detailed information about the symptoms, causes, and treatments of Miyoshi myopathy is available below.

Symptoms of Miyoshi myopathy

Miyoshi myopathy: Related Patient Stories

Miyoshi myopathy: Complications

Read more about complications of Miyoshi myopathy.

Causes of Miyoshi myopathy

Read more about causes of Miyoshi myopathy.

Disease Topics Related To Miyoshi myopathy

Research the causes of these diseases that are similar to, or related to, Miyoshi myopathy:

Less Common Symptoms of Miyoshi myopathy

Miyoshi myopathy: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Evidence Based Medicine Research for Miyoshi myopathy

Medical research articles related to Miyoshi myopathy include:

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

Miyoshi myopathy: Animations

Prognosis for Miyoshi myopathy

Prognosis for Miyoshi myopathy: bedridden in about 15 years

Research about Miyoshi myopathy

Visit our research pages for current research about Miyoshi myopathy treatments.

Statistics for Miyoshi myopathy

Miyoshi myopathy: Broader Related Topics

User Interactive Forums

Read about other experiences, ask a question about Miyoshi myopathy, or answer someone else's question, on our message boards:

Definitions of Miyoshi myopathy:

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

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Miyoshi myopathy as a "rare disease".
Source - Orphanet

 

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