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What test should be done to diagnosis PNE? I have read that a regularRegular insulin EMG does work to detect PNE and that I should have PNTML ,Pudenal Terminal Motor Latencie test. Is that a test that a general neurologist is familar with or do I need to see a particular kind of neurologist?
Hi
Thanks for writing to the forum!
A neurologist will usually follow four steps to diagnosis. “The predominant factorFactor ix complex in the diagnoses of pudendal neuralgiaCluster headaches Neuralgia Trigeminal neuralgia are the symptoms.
Then, the medical exams that one should have are:
1. The clinical exam
2. MRI or CT Scan
3. Pudendal NerveNerve biopsy Nerve conduction velocity Motor Latency Test (PNMLT)
4. Diagnostic block”
Hope this helps. You can refer to this link for more details: http://www.pudendal.info/info/DiagnosisInfo.htm
Do most neurologist do PNMLT testing? I called one nuerologist and I told him I may have PNE and he said not to make an appointment with him that was not his expertise.
At least he was honest about it. Should I just ask if they treat Pudendal NeuralgiaCluster headaches Neuralgia Trigeminal neuralgia? My symptoms fit that description even though I know it could be other things. It would be nice to have a professional person like a DR do some more definitive studies before we rule it in or out. Would and Orthopedist be a better choice specialist?
Hi
Thanks for keeping me posted!
Yes, true. You should be evaluated. This is a littleLittle noses decongestant Little tummys known problem—not common. I am providing you with a link where you can get all the information you need, a list od doctors treating it, clinics where treatment is available-etc. Hoe you find this useful.
Refer: http://www.pudendalhelp.com/
I Please let me know if there is any thing else and do keep me posted. Take care!
Thanks for writing to the forum!
A neurologist will usually follow four steps to diagnosis. “The predominant factor in the diagnoses of pudendal neuralgia are the symptoms.
Then, the medical exams that one should have are:
1. The clinical exam
2. MRI or CT Scan
3. Pudendal Nerve Motor Latency Test (PNMLT)
4. Diagnostic block”
Hope this helps. You can refer to this link for more details: http://www.pudendal.info/info/DiagnosisInfo.htm
At least he was honest about it. Should I just ask if they treat Pudendal Neuralgia? My symptoms fit that description even though I know it could be other things. It would be nice to have a professional person like a DR do some more definitive studies before we rule it in or out. Would and Orthopedist be a better choice specialist?
Thanks for keeping me posted!
Yes, true. You should be evaluated. This is a little known problem—not common. I am providing you with a link where you can get all the information you need, a list od doctors treating it, clinics where treatment is available-etc. Hoe you find this useful.
Refer: http://www.pudendalhelp.com/
I Please let me know if there is any thing else and do keep me posted. Take care!