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Anyone have the FGFR3 antibody gene?
Neuropathy | Last Active: Apr 7 6:29pm | Replies (146)Comment receiving replies
Hello @darlia, welcome to Mayo Connect. We are happy you found us. Connect is a great place to ask questions, share your story and learn from others with similar health issues. I'm hoping someone else has information they can share with you on the FGFR3 antibody gene. I had not heard of it as a cause for neuropathy. I did a search and found the following information:
National Institutes of Health - Antifibroblast growth factor receptor 3 antibodies identify a subgroup of patients with sensory neuropathy.
https://www.ncbi.nlm.nih.gov/pubmed/25628376
I also did a search using Google Scholar (https://scholar.google.com/) which is great for finding research articles. I used "fgfr3 clinical trials" for the search phrase and it came up with the following links:
https://scholar.google.com/scholar?hl=en&q=fgfr3+clinical+trials&btnG=&as_sdt=1%2C24&as_sdtp=
On the Google Scholar search engine you can refine your search to the most recent information by clicking the year 2017 on the left side of the window.
Did the neurologist give you the "idiopathic" diagnosis? I have idiopathic small fiber neuropathy but only have the numbness in my legs and feet. I do take some natural supplements and vitamins that appears to have stopped the progression. Here is a bookmark link to my story I shared in another post on Connect:
https://connect.mayoclinic.org/comment/65985/bookmark/?ajax_hook=action&_wpnonce=13af2ed380
John
Replies to "Hello @darlia, welcome to Mayo Connect. We are happy you found us. Connect is a great..."
I can understand your concerns. You have a lot on your plate. I did another search on Google Scholar for IV SOLU MEDROL treatment side effects and it has some information but I'm not sure it's what you are looking for:
https://scholar.google.com/scholar?hl=en&as_sdt=0,24&q=IV+SOLU+MEDROL+treatment+side+effects
Thank you so much for the help! I will read all of this when I have a chance.
Darlia
I need to take time to look at the vitamins you suggest. Or if you can list them briefly here that would be great!
Also I want to answer the ? About idiopathic. I found out that term means that the origin is unknown.
Mine was until the discovery of the FGFR3 ANTIBODY. THIS IS THE SUPPOSED CAUSE.
For others out there. Ask to have your blood tested for this. Not all labs can do it. Mine was sent to a big University. Check in your area .
Darlia
I see this is an old thread, but the question asked alerted me to two things found on my blood word, Borderline B-12 (for which I am now taking B-12, 3000 mcg, sublingual), and an elevated anti-HDS which is actually associated with atonal sensory neuropathies. The sensory neuropathy has been my operating diagnosis. I could not find any info on-line about possible treatment for the elevated anti-HSD. Is there any information you have on this? Thanks.
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Thank you John for the reply and the welcome. I was researching on the Mayo Clinic website because I have paperwork I am filing out for my attorney here in Missouri where I live now on my SS disability case and I had gone to the Mayo Clinic as a patient when I lived in the Phoenix area for many years. They want you to list your prior medical help so I listed Mayo. I then saw that there was the support community and decided to give it a try. I was told by my Neurologist whom I see here at the University of Missouri Hospital in Columbia, MO, that my neuropathy is FGFR3 Neuropathy, but had been told prior that after my nerve tests it is Peripheral Neuropathy. I have in my feet and legs. It started in my left leg just randomly as a spot on my left calf that was kind of numb. That was back in 2011 or 2012 I believe. It has progressed to my heels being numb in spots and into parts of my feet, mostly the left. Now my hands are having tingling on and off too. My right leg has a little, but not much as of yet. The only treatment I have been told so far that there is as this is a rare condition and that the medical community has just been made aware of this in the last 2 years, he said, is an IV SOLUMEDROL steroid that he wants to do for 6 months and then says I won't even see any diff until at least 2 yrs!. Or there is another treatment that involves being administered by IV that has fractions of blood, immunogentherapy or something. I spelled it wrong. Anyway, it is not an option for me because the treatment is likely to cause renal failure and I only have one kidney as I am a cancer survivor to have lost my right kidney to renal cell carcinoma in 2008. So, at this point, he says that the steroids are the only treatment. I asked what if I DID NOTHING? He says, well then for sure it will just progress. The steroid treatment though is not a guarantee of help either, it is kind of a shot or chance. I also have the gastroparesis which until now had an unknown source because I am pre-diabetic, but NOT diabetic. Normally GASTROPARESIS happens because of diabetes. So, if I don't do anything, this condition is just probably going to get worse, The downside is that I have to watch everything I eat, most of the time, I am pretty good, but it is hard to not eat any raw veggies or fruit until they are broken down like in a smoothy which is ok. The key is to have the food already broken down, I eat pouches of baby food, which surprisingly is pretty good nowadays. LOL. I like the fruity/sweetpotato ones or the fruit mixed with other veggies. I also like from Walmart the Organic SuperFood dehydrated fruits and veggies and probiotics mix. It is very green and it has good spirilina and alphalfa in it. I mix it in Pineapple or Grape Juice. I get my vitamins that way too.
So, right now I am waiting to get an abdominal MRI and checked out out by the Nephrologist that my one kidney is okay to undergo the start of the steroid treatment. But in the meantime, I am searching for other help. Reading about the side effects of the steroidal treatment is scarey and I am very reluctant to do it. Any info you can provide on this would be much appreciated. Thanks again!
Darlia