What age group does Charcot-Marie-Tooth disease affect?
Hear this out loudPauseThe symptoms of CMT usually start to appear between the ages of 5 and 15, although they sometimes do not develop until well into middle age or later. CMT is a progressive condition.
How long is the average lifespan of a person with Charcot-Marie-Tooth disease?
Hear this out loudPauseIn most affected individuals, however, Charcot-Marie-Tooth disease does not affect life expectancy. Typically, the earliest symptoms of Charcot-Marie-Tooth disease result from muscle atrophy in the feet.
Does 23 and ME test for Charcot-Marie-Tooth?
Hear this out loudPauseCan I use 23andMe genetic testing to see if I have CMT? 23andMe’s genetic testing will not be helpful in detecting CMT. While this type of testing is approved to look for some conditions, such as Bloom syndrome, CMT is not one of them.
Is Charcot-Marie-Tooth disease life threatening?
Hear this out loudPauseCMT isn’t usually life-threatening and rarely affects muscles involved in vital functions like breathing. People with most forms of CMT have a normal life expectancy.
How much does a CMT test cost?
CMT Exam Fees
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How much does Invitae cost?
Hear this out loudPauseYou have the option to pay Invitae directly for your testing, for as low as $99 for NIPS (non-invasive prenatal screening) and $250 for diagnostic testing (to understand an inherited disease, uncover the cause of unexplained symptoms), carrier testing (to determine if you could pass a hereditary condition on to your …
What kind of disease is Charcot Marie Tooth?
Charcot-Marie-Tooth disease (CMT) is the most commonly in- herited neurological disease, with an incidence equal to that of mul- tiple sclerosis (1 in 2,500 people). There are currently 2.8 million people with CMT—so why don’t podiatrists treat more people with this disease?
What happens to your feet if you have CMT?
People with CMT have to be particularly careful because swollen feet and legs can lead to skin breakdown and ulcers. These ulcers may get infected and sometimes lead to loss of the foot or leg (i.e., if they get gangrene).
What are the symptoms of hand muscle weakness in Charcot?
Carter GT, Abresch RT, Fowler WM Jr, Johnson ER, Kilmer DD, McDonald CM. Profiles of neuromuscular diseases. Hereditary motor and sensory neuropathy, types I and II. Am J Phys Med Rehabil. 1995 Sep-Oct. 74 (5 Suppl):S140-9. [Medline].