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02-21-2012, 02:12 PM
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#5 | ||
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Grand Magnate
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Hi,
When you mentioned the PMP22 gene it rang a bell. A person who has CMT type 1A has a duplication of it. If there is a deletion then that would indicate HNPP (Hereditary Neuropathy with Liability to Pressure Palsy). Interesting. Here is a site concerning it. http://www.ncbi.nlm.nih.gov/pubmed/14555828 Also, I do believe IVIG is for autoimmune diseases which the two above are not. What are your symptoms if you care to share. Hope you find the answer and thank you.
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Kitt -------------------------------------------------------------------------------------------------------- "It is what it is." |
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