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Neuronopathy, distal, autosomal recessive, 3

Neuronopathy, distal, autosomal recessive, 3: Introduction

Neuronopathy, distal, autosomal recessive, 3: 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, autosomal recessive, 3 is available below.

Symptoms of Neuronopathy, distal, autosomal recessive, 3

Home Diagnostic Testing

Home medical testing related to Neuronopathy, distal, autosomal recessive, 3:

Wrongly Diagnosed with Neuronopathy, distal, autosomal recessive, 3?

Causes of Neuronopathy, distal, autosomal recessive, 3

Read more about causes of Neuronopathy, distal, autosomal recessive, 3.

Neuronopathy, distal, autosomal recessive, 3: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Neuronopathy, distal, autosomal recessive, 3

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

Neuronopathy, distal, autosomal recessive, 3: Research Doctors & Specialists

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Neuronopathy, distal, autosomal recessive, 3: Animations

Prognosis for Neuronopathy, distal, autosomal recessive, 3

Prognosis for Neuronopathy, distal, autosomal recessive, 3: 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, autosomal recessive, 3: Broader Related Topics

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More information about Neuronopathy, distal, autosomal recessive, 3

  1. Neuronopathy, distal, autosomal recessive, 3: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Prognosis
 

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