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What is Myopathy, hyaline body, autosomal dominant?

What is Myopathy, hyaline body, autosomal dominant?

  • Myopathy, hyaline body, autosomal dominant: A rare form of genetic muscle disease which progresses slowly and causes generalized muscle weakness and wasting. The condition results from the abnormal presence of hyaline bodies in type 1 muscle fibres.

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

Myopathy, hyaline body, autosomal dominant: Introduction

Types of Myopathy, hyaline body, autosomal dominant:

Broader types of Myopathy, hyaline body, autosomal dominant:

What causes Myopathy, hyaline body, autosomal dominant?

Causes of Myopathy, hyaline body, autosomal dominant: see causes of Myopathy, hyaline body, autosomal dominant

What are the symptoms of Myopathy, hyaline body, autosomal dominant?

Symptoms of Myopathy, hyaline body, autosomal dominant: see symptoms of Myopathy, hyaline body, autosomal dominant

Onset of Myopathy, hyaline body, autosomal dominant: Any age from first to the fifth decade of life.

How is it treated?

Treatments for Myopathy, hyaline body, autosomal dominant: see treatments for Myopathy, hyaline body, autosomal dominant

Name of Myopathy, hyaline body, autosomal dominant

Main name of condition: Myopathy, hyaline body, autosomal dominant

 

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