If you can’t detox ammonia via the liver the brain and muscle can be utilised(2:20) and exercise increases the problem 3 fold (10:40)
Would ammonia effect platelets as well
I’m wondering if I may have something like partial NAGS deficiency (slc13a3) and found this on very rare urea cycle disorders
http://www.nucdf.org/documents/NORD_Physician_Guide_to_Urea_Cycle_Disorders.pdf
Pyruvate in general has been mentioned before in M.E
Fluge and mella
Ron Davis pyruvate normalises blood and so does copaxone
And dr bhupesh prusty mentions PDP1
It raised my interest as I likely have a deficiency at PDP2 and something happening with a-ketogluterate in urine glutamate and...
One of the hallmarks was that it was a cluster outbreak very few mecfs are part of a cluster outbreak these days
Could it of been a coronavirus in evolution at the outbreaks
I remember some link to Far East as well
https://www.newsmax.com/t/newsmax/article/968688?section=us&keywords=ivermectin-drug-virus&year=2020&month=05&date=22&id=968688&oref=r.search.yahoo.com
I wonder if ivermectin works in a similar way to suramin
Then the counter argument...
If you have genes related to dementia risk (APOE)ect,are you more likely to develop M.E
And severe COVID as a few papers have suggested.
https://www.sciencemediacentre.org/expert-reaction-to-study-on-covid-19-and-a-faulty-gene-linked-to-dementia/
I may have risk due to PITX2 but I think this...
PITX2 activates PDP2 so theoretically I’ll have low pyruvate dehydrogenase as I have a point mutation in PITX2
https://iovs.arvojournals.org/article.aspx?articleid=2385923
And SLC13A3
https://iovs.arvojournals.org/article.aspx?articleid=2364484
Are these classed as inborn errors of metabolism or mitochondrial disorders
Is high or low glutamate a feature
n-carbamyglutamate (carglumic acid) as treatment
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