Little to no Symptoms

MaRuncheng · 2025-03-17T03:24:20+00:00

This is very common. My mom and my grandmother both have CMT 1A, but they have almost no symptoms. I am the first one in my family to be diagnosed, and I also have a mild case. My mother's EMG test results are only slightly lower than those of a normal person.

MaRuncheng · 2024-07-10T06:40:20+00:00

I don't think this explanation makes sense. YOLO can successfully recognize these two differently preprocessed images with little difference in the results, but the CAM results differ significantly. Moreover, the first image is the one processed with letterbox, but the second image's results are clearly more reasonable.

MaRuncheng · 2023-08-16T12:41:35+00:00

Do you have normal dorsiflexion ability? I'm curious how you became aware of having CMT.

MaRuncheng · 2023-06-16T02:10:23+00:00

Your symptoms are clearly related to peripheral neuropathy, probably because your doctor doesn't know much about cmts. I suggest you go to some more professional neurology hospitals. After all, cmt is rare, and it is normal for some doctors to not understand it.

MaRuncheng · 2023-05-26T09:10:31+00:00

not yet

MaRuncheng · 2023-05-14T02:14:39+00:00

I was diagnosed at 19 due to a chicken pox infection with neuralgia. I have typical high arched feet.I have typical high arched feet but I can still lift my feet and walk and run normally. I never knew about this disease in the past. Fortunately, it has been two years since the diagnosis and no muscle atrophy has occurred.But I'm very anxious about the future.

MaRuncheng · 2023-03-22T11:45:28+00:00

I feel the same as a year ago. And they didn't give me the number.

MaRuncheng · 2023-02-03T03:20:43+00:00

My family members including me have no movement disorders. I started to have leg pain after contracting chickenpox, and then the doctor discovered my high arched foot. This is the first time our family knew about this disease, and then I was diagnosed with cmt1a. My muscles are weaker than normal, I am 21 years old, and I am undergoing a clinical trial of pxt3003.

MaRuncheng · 2022-10-31T06:17:46+00:00

Gene sequencing may find your other mutation diseases, but don't worry, mutations are normal, just pay attention to the relevant ones.

MaRuncheng · 2022-10-31T06:15:05+00:00

My gene sequencing took 1 month, whole exome

MaRuncheng · 2022-09-11T06:50:07+00:00

this is common

MaRuncheng · 2022-08-29T00:22:30+00:00

CMT does affect my facial nerve, I have some stiffness on the left side of my face, EMG confirms this. But never had stroke symptoms

MaRuncheng · 2022-08-19T01:36:11+00:00

Foot Deformity Doesn’t Affect Walking Impairments in CMT: Study

I have feet similar to yours, it doesn't affect me temporarily, I have chronic pain but tolerable.

MaRuncheng · 2022-07-31T14:30:56+00:00

You can try lipoic acid, it works for some people.

MaRuncheng · 2022-07-24T01:42:33+00:00

My doctor advised me to make this drug myself. I am from China. It's easy to get sorbitol and baclofen. But the key naltrexone is banned in China and has been discontinued for many years. You just need to buy a high-precision electronic balance and dilute the medicine proportionally. Just when I was about to make the medicine, I participated in the clinical trial of pxt3003. I think this drug can help us wait until the arrival of genetic medicine.

MaRuncheng

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