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Member
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Join Date: May 2013
Posts: 135
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Member
Join Date: May 2013
Posts: 135
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It was easy enough to find a program for methylation mutations, but since they shut down the medical analysis arm of 23&me in 2013, how do we now go about researching or raw genetic data? For me, especially how it pertains to PN?
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Idiopathic Sensorimotor Polyneuropathy
Atypical Migraine
Chiari 1 malformation 7 mm
PLIF L5-S1 Sept. 2013
Lumbar MRI March 2013: degenerative changes from L3 to S1. L3 and L4 have tiny annular tears with disc bulge. L5-S1 bilateral pars defects anterolisthesis (spondylosis/spondylithesis?) I have an annular tear here too, along with a conjoined left L5-S1 nerve root. Mild effacement of the thecal sac at the origins of the bilateral S1 nerve roots, left greater than right. Mild bilateral Neural foraminal stenosis.
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