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Spastic paraplegia 19, autosomal dominant

Spastic paraplegia 19, autosomal dominant: Introduction

Spastic paraplegia 19, autosomal dominant: A rare genetic disorder characterized mainly by progressive spasticity and weakness of the lower legs. The condition is generally slow progressing with wheelchair confinement occurring only rarely. More detailed information about the symptoms, causes, and treatments of Spastic paraplegia 19, autosomal dominant is available below.

Symptoms of Spastic paraplegia 19, autosomal dominant

Home Diagnostic Testing

Home medical testing related to Spastic paraplegia 19, autosomal dominant:

Wrongly Diagnosed with Spastic paraplegia 19, autosomal dominant?

Causes of Spastic paraplegia 19, autosomal dominant

Read more about causes of Spastic paraplegia 19, autosomal dominant.

Spastic paraplegia 19, autosomal dominant: Undiagnosed Conditions

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Misdiagnosis and Spastic paraplegia 19, autosomal dominant

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Spastic paraplegia 19, autosomal dominant: Research Doctors & Specialists

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Spastic paraplegia 19, autosomal dominant: Animations

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Spastic paraplegia 19, autosomal dominant: Broader Related Topics

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Definitions of Spastic paraplegia 19, autosomal dominant:

Spastic paraplegia 19, 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 Spastic paraplegia 19, autosomal dominant, or a subtype of Spastic paraplegia 19, autosomal dominant, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Related Spastic paraplegia 19, autosomal dominant Info

More information about Spastic paraplegia 19, autosomal dominant

  1. Spastic paraplegia 19, autosomal dominant: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
 

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