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Charcot-Marie-Tooth, demyelinating, autosomal recessive

Charcot-Marie-Tooth, demyelinating, autosomal recessive: Introduction

Charcot-Marie-Tooth, demyelinating, autosomal recessive: 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 4 has an autosomal recessive form of inheritance and is a severe form of the disease. More detailed information about the symptoms, causes, and treatments of Charcot-Marie-Tooth, demyelinating, autosomal recessive is available below.

Symptoms of Charcot-Marie-Tooth, demyelinating, autosomal recessive

Home Diagnostic Testing

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Wrongly Diagnosed with Charcot-Marie-Tooth, demyelinating, autosomal recessive?

Causes of Charcot-Marie-Tooth, demyelinating, autosomal recessive

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Charcot-Marie-Tooth, demyelinating, autosomal recessive: Undiagnosed Conditions

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Misdiagnosis and Charcot-Marie-Tooth, demyelinating, autosomal recessive

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...read more »

Charcot-Marie-Tooth, demyelinating, autosomal recessive: Research Doctors & Specialists

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Hospitals & Clinics: Charcot-Marie-Tooth, demyelinating, autosomal recessive

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Charcot-Marie-Tooth, demyelinating, autosomal recessive: Animations

Charcot-Marie-Tooth, demyelinating, autosomal recessive: Broader Related Topics

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More information about Charcot-Marie-Tooth, demyelinating, autosomal recessive

  1. Charcot-Marie-Tooth, demyelinating, autosomal recessive: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
 

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