Guest guest Posted January 13, 2010 Report Share Posted January 13, 2010 Hi, I first learned about the methylenetetrahydrofolate reductase (MTHFR) gene on this group, so I thought I would post my question here. First off, my son is going to his first DAN! appt in about a week. I assume they will test his urine, hair, blood, etc. One thing for sure is that he is doing really well with taking digestive enzymes. This makes me think that he's got a problem with creating his own digestive enzymes for reasons currently unknown. One of the reasons might be mercury, could be viral stuff, low-level bacterial stuff ... but then there's that new thing I read about here .... MTHFR ... which maybe can be picked up initially via urine analysis? Anyway, it occurred to me tonight that my son has these ASD thingies going on. Then, there's my daughter who has Chiari Malformation Type I, which is a congenital problem, related to neural tube defects. I google'd it and MTHFR mutations are associated with Chiari Malformation. (see this article, although there are others: http://www.springerlink.com/content/hrqlfp1qgj5tle9c/ Anyway, has anyone else researched this already? Or, do you have 2 children that have ASD and/or Chiari or spina bifida or tethered cord or any sort of other neural tube defect type)? It sure would be interesting if I find the missing " link " here on my two sweeties. Quote Link to comment Share on other sites More sharing options...
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