التفاصيل البيبلوغرافية
| العنوان: |
Distal motor axonal dysfunction in amyotrophic lateral sclerosis |
| المؤلفون: |
Noto, Yu-ichi1,2 y-noto@koto.kpu-m.ac.jp, Kanai, Kazuaki1, Misawa, Sonoko1, Shibuya, Kazumoto1, Isose, Sagiri1, Nasu, Saiko1, Sekiguchi, Yukari1, Fujimaki, Yumi1,3, Nakagawa, Masanori2, Kuwabara, Satoshi1 |
| المصدر: |
Journal of the Neurological Sciences. Mar2011, Vol. 302 Issue 1/2, p58-62. 5p. |
| مصطلحات موضوعية: |
*AMYOTROPHIC lateral sclerosis, *MOTOR neuron diseases, *AXONS, *NEURAL conduction, *NEUROPATHY, *NEURODEGENERATION, *PATHOLOGICAL physiology, *EXCITATION (Physiology) |
| مستخلص: |
Abstract: Nerve conduction slowing in amyotrophic lateral sclerosis (ALS) is usually caused by loss of fast motor axons. We studied the frequency, extent, and distribution of prominently prolonged distal motor latencies in ALS. We reviewed results of median, ulnar, and tibial nerve conduction studies in 91 patients with ALS, 24 with lower motor neuron disorders, and 36 with axonal neuropathy. Coincidental carpal tunnel syndrome was found for 4 (4.4%) of the ALS patients who were excluded from analyses. Markedly prolonged distal latencies (>125% of the upper limit of normal) were found only in the median nerve of ALS patients (9%), and in none of the disease controls. Excitability studies suggested membrane depolarization in some ALS patients. Our results show that approximately 10% of ALS patients shows prominently prolonged median distal latency, which cannot be explained by axonal loss and carpal tunnel lesion. The distal nerve conduction slowing may partly be caused by membrane depolarization possibly due to motor neuronal degeneration in ALS. We suggest that recognition of the pattern of distal motor axonal dysfunction predominant in the median nerve is clinically important, and could provide additional insights into the pathophysiology of ALS. [Copyright &y& Elsevier] |
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