Guest guest Posted November 5, 2004 Report Share Posted November 5, 2004 I've finally received a callback from my " neurologist with apparent interest in mito " at MGH. His office left a message about the test they want to do, so I wasn't able to ask any questions yet. BTW I had NO idea how many calls and delays would be required, before I could get this simple next step rolling. What they want to do, they called it " mitochondrial myopathy DNA evaluation " and then said this is " blood work " . I have a definite diagnosis of MSL which is known to have mito origins (and for which SOME patients have various KNOWN particular mtDNA mutations). I have not yet had any DNA tests or biopsies. FWIW they also want to do an EMG (presumably far more involved than one I had three years ago). Before I call them back on Monday to schedule this test, does anyone have any specific questions I should ask, or " suggestions " as to which specific DNA tests should be done, or preferred labs to do the testing (I think they do at least some of this in-house, but I don't really know)? I have the feeling that I will have little input on any of this, but it's worth a try. Presumably the results may lead to further testing. Thanks in advance Steve D. Quote Link to comment Share on other sites More sharing options...
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