Charcot-Marie-Tooth Disease (CMT)

A Guide to Understanding Hereditary Motor and Sensory Neuropathy

Neurology

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Last updated: Mar 24, 2025

What is CMT?

Charcot-Marie-Tooth disease (CMT) is an inherited neurological disorder that affects the peripheral nerves, which carry signals between your brain and spinal cord to your muscles and sensory organs.

Key Characteristics

  • Progressive muscle weakness
  • Decreased muscle mass (atrophy)
  • Reduced sensation in feet, legs, hands, and arms
  • High-arched feet (pes cavus)
  • Foot deformities

Types of CMT

Type 1 (CMT1)

  • Most common form
  • Slow nerve conduction
  • Symptoms typically begin in childhood

Type 2 (CMT2)

  • Normal or near-normal nerve conduction
  • Later onset of symptoms

Other Types

  • X-linked
  • Type 3 (Dejerine-Sottas disease)
  • Type 4

Common Symptoms

Early Signs

  • Frequent tripping or falling
  • Awkward gait
  • Foot drop

Progressive Symptoms

  • Muscle wasting in legs and feet
  • Decreased ability to feel heat, cold, and touch
  • Hand weakness and decreased fine motor skills
  • Balance problems

Diagnosis

  1. Physical examination
  2. Family history review
  3. Nerve conduction studies
  4. Genetic testing
  5. EMG (electromyography)

Treatment Options

Physical Therapy

  • Muscle strengthening exercises
  • Stretching routines
  • Balance training

Occupational Therapy

  • Adaptive techniques for daily activities
  • Equipment recommendations

Orthopedic Devices

  • Ankle braces
  • Custom footwear
  • Walking aids

Living with CMT

Self-Care Strategies

  • Regular exercise within capabilities
  • Proper foot care
  • Weight management
  • Safety precautions

When to Contact Healthcare Provider

  • Increased weakness
  • New balance problems
  • Unexpected pain
  • Changes in sensation

Research and Future Prospects

  • Ongoing genetic research
  • Clinical trials
  • Emerging therapies

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