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11-13-2014, 02:23 PM
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Just ordered my genetic test kit. I will have to see how to get an interpretation of raw data, but I know where to upload the report, once I have it, to find my methylation profile. I'm not so keen on finding relatives in some distant part of the world, as I am to find the causes of my neurological problems.
Has anyone got experience with genetic tests? And with their interpretation?
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Multifocal motor neuropathy with conduction block since late 2005, diagnosed 12 November 2014 |
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| "Thanks for this!" says: | DejaVu (08-23-2015) |
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11-13-2014, 04:05 PM
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I ran mine through Genetic Genie. It provided some explanation with my mutations that pointed me in a direction to follow for dietary changes/supplements. Can't link it here for you but you can Google it.
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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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11-13-2014, 04:08 PM
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That one is on my list, thanks. Hope their explanations were clear enough. I know exactly nothing about genetic issues and I don't think I will have appetite or time to study it extensively :P
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Multifocal motor neuropathy with conduction block since late 2005, diagnosed 12 November 2014 |
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| "Thanks for this!" says: | DejaVu (08-23-2015) |
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11-13-2014, 04:25 PM
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Wisest Elder Ever
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This is a start.
http://www.snpedia.com/index.php/SNPedia There is a poster on PN who looked up SNPs. I'll look for her posts, later.
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All truths are easy to understand once they are discovered; the point is to discover them.-- Galileo Galilei ************************************ . Weezie looking at petunias 8.25.2017 **************************** These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here.
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11-13-2014, 04:41 PM
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Wisest Elder Ever
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__________________
All truths are easy to understand once they are discovered; the point is to discover them.-- Galileo Galilei ************************************ . Weezie looking at petunias 8.25.2017 **************************** These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here.
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11-13-2014, 05:03 PM
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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?
__________________
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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| "Thanks for this!" says: | DejaVu (08-23-2015) |
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