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Charcot-Marie-Tooth disease, Type 2AII

Charcot-Marie-Tooth disease, Type 2AII: Introduction

Charcot-Marie-Tooth disease, Type 2AII: CMT is an inherited neurological disease characterized by the gradual degeneration of nerves which starts in the hands and feet and results in progressive numbness, muscle weakness and loss of function. Type 2A2 has an autosomal dominant inheritance and involves a defect in the MFN2 gene on chromosome 1p36. More detailed information about the symptoms, causes, and treatments of Charcot-Marie-Tooth disease, Type 2AII is available below.

Symptoms of Charcot-Marie-Tooth disease, Type 2AII

Home Diagnostic Testing

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Wrongly Diagnosed with Charcot-Marie-Tooth disease, Type 2AII?

Causes of Charcot-Marie-Tooth disease, Type 2AII

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Charcot-Marie-Tooth disease, Type 2AII: Undiagnosed Conditions

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Misdiagnosis and Charcot-Marie-Tooth disease, Type 2AII

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...read more »

Charcot-Marie-Tooth disease, Type 2AII: Research Doctors & Specialists

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Hospitals & Clinics: Charcot-Marie-Tooth disease, Type 2AII

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Charcot-Marie-Tooth disease, Type 2AII: Animations

Charcot-Marie-Tooth disease, Type 2AII: Broader Related Topics

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Related Charcot-Marie-Tooth disease, Type 2AII Info

More information about Charcot-Marie-Tooth disease, Type 2AII

  1. Charcot-Marie-Tooth disease, Type 2AII: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
 

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