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Charcot-Marie-Tooth disease deafness recessive type

Charcot-Marie-Tooth disease deafness recessive type: Introduction

Charcot-Marie-Tooth disease deafness recessive type: 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 4D is inherited recessively and is caused by a defected in a gene in chromosome 8 and is a severe form of the disease that also involves deafness. More detailed information about the symptoms, causes, and treatments of Charcot-Marie-Tooth disease deafness recessive type is available below.

Symptoms of Charcot-Marie-Tooth disease deafness recessive type

Home Diagnostic Testing

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Wrongly Diagnosed with Charcot-Marie-Tooth disease deafness recessive type?

Causes of Charcot-Marie-Tooth disease deafness recessive type

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Charcot-Marie-Tooth disease deafness recessive type: Undiagnosed Conditions

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Misdiagnosis and Charcot-Marie-Tooth disease deafness recessive type

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Charcot-Marie-Tooth disease deafness recessive type: Research Doctors & Specialists

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Hospitals & Clinics: Charcot-Marie-Tooth disease deafness recessive type

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Charcot-Marie-Tooth disease deafness recessive type: Rare Types

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Charcot-Marie-Tooth disease deafness recessive type: Animations

Charcot-Marie-Tooth disease deafness recessive type: Broader Related Topics

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Related Charcot-Marie-Tooth disease deafness recessive type Info

More information about Charcot-Marie-Tooth disease deafness recessive type

  1. Charcot-Marie-Tooth disease deafness recessive type: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Types
 

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