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Dystonia 15, myoclonic

Dystonia 15, myoclonic: Introduction

Dystonia 15, myoclonic: A rare genetic movement disorder. The muscles contract involuntarily causing repetitive twisting and jerking movements. Type 15 is caused by a genetic defect on chromosome 18p11. More detailed information about the symptoms, causes, and treatments of Dystonia 15, myoclonic is available below.

Symptoms of Dystonia 15, myoclonic

Home Diagnostic Testing

Home medical testing related to Dystonia 15, myoclonic:

Wrongly Diagnosed with Dystonia 15, myoclonic?

Causes of Dystonia 15, myoclonic

Read more about causes of Dystonia 15, myoclonic.

Less Common Symptoms of Dystonia 15, myoclonic

Dystonia 15, myoclonic: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Dystonia 15, myoclonic

Vitamin B12 deficiency under-diagnosed: The condition of Vitamin B12 deficiency is a possible misdiagnosis of various conditions, such as multiple sclerosis (see symptoms of multiple sclerosis). See symptoms of...read more »

Dystonia 15, myoclonic: Research Doctors & Specialists

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Dystonia 15, myoclonic: Animations

Statistics for Dystonia 15, myoclonic

Dystonia 15, myoclonic: Broader Related Topics

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Definitions of Dystonia 15, myoclonic:

Dystonia 15, myoclonic is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Dystonia 15, myoclonic, or a subtype of Dystonia 15, myoclonic, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Related Dystonia 15, myoclonic Info

More information about Dystonia 15, myoclonic

  1. Dystonia 15, myoclonic: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
 

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