Charcot-Marie-Tooth disease with pyramidal features- autosomal dominant
Overview
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
Symptoms
* Wasted peroneal muscles * Walking difficulty * Wasted muscles in extremities * Weak muscles in extremities * Absent reflexes * Loss of sensation in limbs * High foot arch * Hammer toes * Increased muscle tone * Spastic dysphonia * Movement disorders
Diagnosis
This medical information about signs and symptoms for Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant has been gathered from various sources, may not be fully accurate, and may not be the full list of Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant signs or Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant symptoms. Furthermore, signs and symptoms of Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant may vary on an individual basis for each patient. Only your doctor can provide adequate diagnosis of any signs or symptoms and whether they are indeed Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant symptoms.