Keyword Analysis & Research: cmt

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Frequently Asked Questions

Is CMT a genetic disease?

The gene mutations in CMT disease are usually inherited. Each of us normally possesses two copies of every gene, one inherited from each parent. Some forms of CMT are inherited in an autosomal dominant fashion, which means that only one copy of the abnormal gene is needed to cause the disease.

What is CMT in medical terms?

Medical Definition of Charcot-Marie-Tooth disease. The disease can be inherited as an autosomal dominant trait, an autosomal recessive trait, or an X-linked trait. There are also sporadic cases in which there is no family history due to a new dominant mutation. Abbreviated CMT. Also known as peroneal muscular atrophy and hereditary motor and sensory neuropathy.

What is the full form of CMT?

Full Form of CMT is Export Business. CMT Stands for Cut, Make and Trims. CMT is a costing procedure of garment making and a how to deal with suppliers. It includes cutting cost, sewing cost and finishing cost. Another way to quote pricing to buyer is FOB.

How to diagnose CMT?

To diagnose CMT, your doctor will order tests to help determine the cause and extent of your nerve damage. These tests may include a nerve conduction study, electromyography, nerve biopsy, and genetic testing. A nerve conduction study can test the function of electrical signals in your nerves.

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