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Neuronopathy, distal hereditary motor, type IV

Neuronopathy, distal hereditary motor, type IV: Introduction

Neuronopathy, distal hereditary motor, type IV: An inherited neuromuscular disease that causes progressive muscle wasting and weakness in the limbs without any sensory impairment. HMN III and HMN IV are forms of autosomal recessive distal neuronopathy type 3 - the only difference is that HMN III is a slightly milder version. More detailed information about the symptoms, causes, and treatments of Neuronopathy, distal hereditary motor, type IV is available below.

Symptoms of Neuronopathy, distal hereditary motor, type IV

Home Diagnostic Testing

Home medical testing related to Neuronopathy, distal hereditary motor, type IV:

Wrongly Diagnosed with Neuronopathy, distal hereditary motor, type IV?

Causes of Neuronopathy, distal hereditary motor, type IV

Read more about causes of Neuronopathy, distal hereditary motor, type IV.

Neuronopathy, distal hereditary motor, type IV: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Neuronopathy, distal hereditary motor, type IV

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

Neuronopathy, distal hereditary motor, type IV: Research Doctors & Specialists

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Neuronopathy, distal hereditary motor, type IV: Animations

Prognosis for Neuronopathy, distal hereditary motor, type IV

Prognosis for Neuronopathy, distal hereditary motor, type IV: The condition is slowly progressive and the legs tend to be more affected than the arms. Eventually weak diaphragmatic muscles can affect breathing.

Neuronopathy, distal hereditary motor, type IV: Broader Related Topics

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More information about Neuronopathy, distal hereditary motor, type IV

  1. Neuronopathy, distal hereditary motor, type IV: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Prognosis
 

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