Guest guest Posted December 31, 2002 Report Share Posted December 31, 2002 <A HREF= " http://seattlepi.nwsource.com/local/102183_gene31.shtml " >Scientists strike back at nerve disorder that c…</A> The article starts like this, then has lots of information. At least having a front page spread is a start. One of my friends called to alert me before I'd seen it. Tuesday, December 31, 2002 Scientists strike back at nerve disorder that cost them their dreams By CAROL SMITH SEATTLE POST-INTELLIGENCER REPORTER Phil Chance wanted to be a concert clarinetist. Street hoped to become a veterinarian. A little-understood genetic defect that can cause severe nerve damage cost them their dreams. Today, as University of Washington scientists, they're striking back. In their Seattle lab, the researchers have located one of the key genes that causes Charcot-Marie-Tooth, a hereditary condition affecting the nerves that deliver messages from the spinal cord to the muscles. Their findings, possibly a step toward a cure, will be published in January in the journal Neurology. Although few people have heard of Charcot-Marie-Tooth, it affects as many people as cystic fibrosis. CMT is not a benign disorder, but unlike high-profile diseases such as Alzheimer's or Parkinson's, it hasn't attracted much research interest. Kat Seattle USA http://www.icewindow.com KathleenLS@... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 4, 2003 Report Share Posted January 4, 2003 Thank you so much for this informative article. As with the family in this article my Mothers side of the family has always had high arches and hammer toes and as it turned out they did have CMT but it did not seem to slow any of them down. For me and my brother this news was not so good because my Dad's family has CMT and they found out that both of his parents had it, but my Grandmother had had no problems with it in her life; so until the testing no one knew. We were unable to find out if my Mothers father had it but I guess it really does not matter. I have 4 children and non of them have shown any signs of it so far, but now that we know how easy it is to pass on to our children all of them have been educated about genetics and they stay away from any meds on the no no list just in case. Hugs Lori Quote Link to comment Share on other sites More sharing options...
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