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Inclusion body myopathy, autosomal dominant

Inclusion body myopathy, autosomal dominant: Introduction

Inclusion body myopathy, autosomal dominant: A dominantly inherited muscle wasting disorder in which the thigh muscles are affected first. The rate of progression and severity can vary amongst patients. More detailed information about the symptoms, causes, and treatments of Inclusion body myopathy, autosomal dominant is available below.

Symptoms of Inclusion body myopathy, autosomal dominant

Causes of Inclusion body myopathy, autosomal dominant

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Definitions of Inclusion body myopathy, autosomal dominant:

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

Related Inclusion body myopathy, autosomal dominant Info

More information about Inclusion body myopathy, autosomal dominant

  1. Inclusion body myopathy, autosomal dominant: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
 

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