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

• Progressive muscle weakness
• Difficulty climbing stairs
• Waddling gait
• Lower back pain
• Increased serum creatine kinase
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Causes of Filaminopathy, autosomal dominant

Read more about causes of Filaminopathy, autosomal dominant.

Less Common Symptoms of Filaminopathy, autosomal dominant

• Respiratory insufficiency
• more symptoms...»

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Filaminopathy, autosomal dominant: Research Doctors & Specialists

Research related physicians and medical specialists:

• Muscle and Orthopedic Specialists:
  • Neuromusculoskeletal Medicine
  • Orthopedic Surgery
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Filaminopathy, autosomal dominant: Animations

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Statistics for Filaminopathy, autosomal dominant

• Medical statistics for Filaminopathy, autosomal dominant
• Prevalence and incidence statistics for Filaminopathy, autosomal dominant
• Death and Mortality statistics for Filaminopathy, autosomal dominant
• Society statistics for Filaminopathy, autosomal dominant

Filaminopathy, autosomal dominant: Broader Related Topics

• Genetic conditions
• Muscle conditions
• Musculoskeletal conditions
• more types...»

Types 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)

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