TREATMENTS &
RESEARCH
latest
treatment
information
here.
Dr. Huntley's
Diagnosis
Checklist
See what questions
a doctor would ask.
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
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: 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
Some of the symptoms of Charcot-Marie-Tooth disease, autosomal recessive, type 4G incude:
Search to find out more about Charcot-Marie-Tooth disease, autosomal recessive, type 4G:
|
What do you think about the features of this website? Take our user survey and have your say:
Tools & Services:
Medical Articles:
Search Specialists by State and City
By using this site you agree to our Terms of Use. Information provided on this site is for informational purposes only; it is not intended as a substitute for advice from your own medical team. The information on this site is not to be used for diagnosing or treating any health concerns you may have - please contact your physician or health care professional for all your medical needs. Please see our Terms of Use.
Copyright © 2009 Health Grades Inc. All rights reserved.