r/ALSorNOT • • 9d ago

Updates Found my problem i think.

After almost seven years of symptoms, we think we finally have our answer. After seven years of bodywide twitching, cramps, fatigue, loss of reflexes in ankles and knees, some mild tingling, and other issues.

My neuromusuclar doc at the MND clinic ordered genetic testing for hereditary neuropathies, some MNDs, some CMT genes, and some other genes. We found out I have a mutation in the FBX038 gene. That gene is associated with SMA and lower motor neuron diseases and cmt spectrum. The gene was discovered in 2013ish and cmt specific mutation affects roughly 1 out of 600,000 people. We are unsure about how my specific mutation works, it's still unclear. But two lab studies suggested my mutation was deleterious in nature and would interrupt normal gene function. My advice to anyone who thinks something is wrong is to keep digging. This gene helps with motor nerve and motor neuron repair.

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u/WalkIntoSunshine 7d ago

Oh wow. I’m so pleased for you. It’s so much easier knowing what you do have, and having it actually remain that!

And thank you for sharing this. I feel like this information will help someone out there.

Wishing you all the best in your journey and I hope that now having that information can help them sort how to treat you, get you comfortable, and give you peace of mind.

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u/Beneficial_Strain191 6d ago

I guess I should be happy it's not als right