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Dictionary » Charcot-Marie-Tooth disease, autosomal recessive, type 4G
 

Charcot-Marie-Tooth disease, autosomal recessive, type 4G

Introduction: Charcot-Marie-Tooth disease, autosomal recessive, type 4G

Description of Charcot-Marie-Tooth disease, autosomal recessive, type 4G

Charcot-Marie-Tooth disease, autosomal recessive, type 4G (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 4G has an autosomal recessive form of inheritance and is a severe form of the disease. It involves a defect on Chromosome 10.

See also:

Charcot-Marie-Tooth disease, Type 4G:
  »Introduction: Charcot-Marie-Tooth disease, Type 4G
  »Symptoms of Charcot-Marie-Tooth disease, Type 4G

Charcot-Marie-Tooth disease, autosomal recessive, type 4G: Related Topics

These medical condition or symptom topics may be relevant to medical information for Charcot-Marie-Tooth disease, autosomal recessive, type 4G:

Charcot-Marie-Tooth disease, autosomal recessive, type 4G as a Disease

Charcot-Marie-Tooth disease, autosomal recessive, type 4G: Another name for Charcot-Marie-Tooth disease, Type 4G (or close medical condition association).
  »Introduction: Charcot-Marie-Tooth disease, Type 4G
  »Symptoms of Charcot-Marie-Tooth disease, Type 4G

Symptoms of Charcot-Marie-Tooth disease, autosomal recessive, type 4G (Charcot-Marie-Tooth disease, Type 4G)

Some of the symptoms of Charcot-Marie-Tooth disease, autosomal recessive, type 4G incude:

See full list of 14 symptoms of Charcot-Marie-Tooth disease, autosomal recessive, type 4G (Charcot-Marie-Tooth disease, Type 4G)

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