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Filaminopathy, autosomal dominant

Filaminopathy, autosomal dominant: Introduction

Filaminopathy, autosomal dominant: A rare dominantly inherited muscle disease characterized slow-progressing muscle weakness. The upper legs seemed to be the most affected with the arms being less involved. More detailed information about the symptoms, causes, and treatments of Filaminopathy, autosomal dominant is available below.

Symptoms of Filaminopathy, autosomal dominant

Causes of Filaminopathy, autosomal dominant

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Definitions of Filaminopathy, autosomal dominant:

Filaminopathy, 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 Filaminopathy, autosomal dominant, or a subtype of Filaminopathy, autosomal dominant, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Related Filaminopathy, autosomal dominant Info

More information about Filaminopathy, autosomal dominant

  1. Filaminopathy, autosomal dominant: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
 

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