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Charcot-Marie-Tooth disease, Type 2L

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

Charcot-Marie-Tooth disease, Type 2L: 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 2L has an autosomal dominant inheritance and involves a defect in the HSPB8 gene on chromosome 12. More detailed information about the symptoms, causes, and treatments of Charcot-Marie-Tooth disease, Type 2L is available below.

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

Home Diagnostic Testing

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

Charcot-Marie-Tooth disease, Type 2L: Related Patient Stories

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

Read more about causes of Charcot-Marie-Tooth disease, Type 2L.

Disease Topics Related To Charcot-Marie-Tooth disease, Type 2L

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

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

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 of...read more »

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

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

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Choosing the Best Hospital: More general information, not necessarily in relation to Charcot-Marie-Tooth disease, Type 2L, on hospital performance and surgical care quality:

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

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

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