Peroneal muscular atrophy with pyramidal features, autosomal dominant

Introduction: Peroneal muscular atrophy with pyramidal features, autosomal dominant

Description of Peroneal muscular atrophy with pyramidal features, autosomal dominant

Peroneal muscular atrophy with pyramidal features, autosomal dominant (medical condition): 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 5 has an autosomal dominant inheritance, progresses slowly and involves movement disorders.

See also:

Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant:
  »Introduction: Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant
  »Symptoms of Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant
  »Treatments for Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant

Peroneal muscular atrophy with pyramidal features, autosomal dominant: Related Topics

These medical condition or symptom topics may be relevant to medical information for Peroneal muscular atrophy with pyramidal features, autosomal dominant:

• Peroneal muscular atrophy
• Muscular atrophy (311 causes)
• Autosomal dominant
• Muscular
• Atrophy (311 causes)
• Pyramidal
• Features
• Autosomal
• Dominant

Peroneal muscular atrophy with pyramidal features, autosomal dominant: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Peroneal muscular atrophy with pyramidal features, autosomal dominant is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Peroneal muscular atrophy with pyramidal features, autosomal dominant, or a subtype of Peroneal muscular atrophy with pyramidal features, autosomal dominant, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Peroneal muscular atrophy with pyramidal features, autosomal dominant as a Disease

Peroneal muscular atrophy with pyramidal features, autosomal dominant: Another name for Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant (or close medical condition association).
  »Introduction: Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant
  »Symptoms of Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant
  »Treatments for Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant

Symptoms of Peroneal muscular atrophy with pyramidal features, autosomal dominant (Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant)

Some of the symptoms of Peroneal muscular atrophy with pyramidal features, autosomal dominant incude:

• Wasted peroneal muscles
• Walking difficulty
• Wasted muscles in extremities
• Weak muscles in extremities
• Absent reflexes

See full list of 17 symptoms of Peroneal muscular atrophy with pyramidal features, autosomal dominant (Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant)

Treatments for Peroneal muscular atrophy with pyramidal features, autosomal dominant (Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant)

Treatments for Peroneal muscular atrophy with pyramidal features, autosomal dominant (Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant) include:

• There is no cure for the condition but measures to manage symptoms may include:
• Physical therapy
• Occupational therapy
• Stretching and low impact exercises
• Braces

See full list of 8 treatments for Peroneal muscular atrophy with pyramidal features, autosomal dominant

Treatment of Peroneal muscular atrophy with pyramidal features, autosomal dominant: For more treatment information about Peroneal muscular atrophy with pyramidal features, autosomal dominant, see treatment of Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant (Peroneal muscular atrophy with pyramidal features, autosomal dominant)

Terms associated with Peroneal muscular atrophy with pyramidal features, autosomal dominant:

Terms Similar to Peroneal muscular atrophy with pyramidal features, autosomal dominant:

• Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant
• CMT with pyramidal features
• HMSN V
• Hereditary motor and sensory neuropathy V

Source - NIH

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