Guest guest Posted April 14, 2000 Report Share Posted April 14, 2000 << My thought was to give the children the blood test first, then if cmt shows up (cmt1, etc.) you and your mother would know what you have also without taking the tests. >> But if the family has a type that is not included in the blood tests it won't help. Most types are not included in the current tests. CMT does present problems in children especially when the parents are not given an accurate diagnosis, and the condition is not explained to them. Children appear very clumsy and awkward, and this can become a means of ridicule to their peers. They feel very different when they can't join in sport and games. http://www.CMT.org.uk/ Diagnosis is usually made through a physical examination that includes tests of muscle function and sensory responses, supplemented with a laboratory test (electromyogram) that measures the electrical activity of muscle cells. In addition, a complete family medical history is taken to determine if the patient's disorder is an inherited one. In some cases, nerve and muscle biopsies may be done to enable the physician to confirm the diagnosis, especially when symptoms are very mild and family history of the disease is not apparent. Both electromyography and muscle biopsy tests help to distinguish between the hypertrophic and neuronal types of the disorder. http://www.mda.org.au/index.html Dept. of Neurology, Detroit First, although you may indeed have CMT type 2 the type of CMT cannot be simply diagnosed because of a clinical onset at 23 years of age. There is actually a lot of variability among degrees of weakness and sensory loss in patients with type 1 and type 2. To distinguish between type 1 or type 2 typically requires nerve conduction velocity testing. Most patients that we see with CMT type 1 or type 2 do not lose all feeling in their feet although the disease is slowly progressive. Numbness, pain and temperature sensations are usually mediated or controlled by small nerves, without much myelin, and these tend to be relatively spared in most types of CMT compared to larger nerves which help us localize where our feet are in space and help our balance. However, even this large nerves usually continue to function at some level in most CMT patients. Moreover, as a rule, most patients who don't present with any disability until their 20's tend to have milder courses. High arches and curled toes are typical in CMT . Kat in Seattle Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 14, 2000 Report Share Posted April 14, 2000 Hi Kat, Peggie here. My nephew was recently tested (blood test) for CMT, as he wouldn't agree to have children until he knew if he had it or not. I just didn't have the heart to tell him nor my brother that the blood test would not neccessary tell him if he had it or not! They told him he did not, but don't think they told him that it only showed a couple of types....... since my brother does not have any symtoms, he doesn't know much about CMT, and has never asked..... Re: I'm new here - diagnosing << My thought was to give the children the blood test first, then if cmt shows up (cmt1, etc.) you and your mother would know what you have also without taking the tests. >> But if the family has a type that is not included in the blood tests it won't help. Most types are not included in the current tests. CMT does present problems in children especially when the parents are not given an accurate diagnosis, and the condition is not explained to them. Children appear very clumsy and awkward, and this can become a means of ridicule to their peers. They feel very different when they can't join in sport and games. http://www.CMT.org.uk/ Diagnosis is usually made through a physical examination that includes tests of muscle function and sensory responses, supplemented with a laboratory test (electromyogram) that measures the electrical activity of muscle cells. In addition, a complete family medical history is taken to determine if the patient's disorder is an inherited one. In some cases, nerve and muscle biopsies may be done to enable the physician to confirm the diagnosis, especially when symptoms are very mild and family history of the disease is not apparent. Both electromyography and muscle biopsy tests help to distinguish between the hypertrophic and neuronal types of the disorder. http://www.mda.org.au/index.html Dept. of Neurology, Detroit First, although you may indeed have CMT type 2 the type of CMT cannot be simply diagnosed because of a clinical onset at 23 years of age. There is actually a lot of variability among degrees of weakness and sensory loss in patients with type 1 and type 2. To distinguish between type 1 or type 2 typically requires nerve conduction velocity testing. Most patients that we see with CMT type 1 or type 2 do not lose all feeling in their feet although the disease is slowly progressive. Numbness, pain and temperature sensations are usually mediated or controlled by small nerves, without much myelin, and these tend to be relatively spared in most types of CMT compared to larger nerves which help us localize where our feet are in space and help our balance. However, even this large nerves usually continue to function at some level in most CMT patients. Moreover, as a rule, most patients who don't present with any disability until their 20's tend to have milder courses. High arches and curled toes are typical in CMT . Kat in Seattle ------------------------------------------------------------------------ Get paid for the stuff you know! Get answers for the stuff you don't. And get $10 to spend on the site! http://click.egroups.com/1/2200/7/_/616793/_/955746528/ ------------------------------------------------------------------------ Quote Link to comment Share on other sites More sharing options...
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