Abstract |
Neuropathy with antibodies against myelin-associated glycoproteins (MAG/ SGPG-N) and hereditary sensorimotor neuropathy type 1 (HMSN1) are characterized by chronic demyelination with little conduction block. Electrodiagnostic studies suggest that in HMSN1 conduction slowing occurs uniformly along the nerve, whereas in MAG/ SGPG-N it is predominantly distal. Some but not all previous reports have shown that the terminal latency index (TLI) was useful to distinguish MAG/ SGPG-N from chronic idiopathic demyelinating polyneuropathy. We compared median TLI from 21 patients with MAG/ SGPG-N with those obtained from 26 patients with HMSN1, 20 with HMSN2, and 12 healthy volunteers. All patients with TLI <0.26 had MAG/ SGPG-N, and all patients with TLI > or =0.32 had HMSN1. In the remaining patients with intermediate TLI values, ulnar distal motor latency (DML) aided in differentiation between MAG/ SGPG-N and HMSN1 with an overall sensitivity of 100% and specificity of 98%. In conclusion, median TLI in combination with ulnar DML can further guide the demyelinating neuropathy evaluation toward hereditary or autoimmune causes.
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Authors | Vitalie D Lupu, Carlos A Mora, Jim Dambrosia, Jacob Meer, Marinos Dalakas, Mary Kay Floeter |
Journal | Muscle & nerve
(Muscle Nerve)
Vol. 35
Issue 2
Pg. 196-202
(Feb 2007)
ISSN: 0148-639X [Print] United States |
PMID | 17068765
(Publication Type: Comparative Study, Journal Article, Research Support, N.I.H., Intramural)
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Chemical References |
- Antibodies
- Myelin-Associated Glycoprotein
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Topics |
- Action Potentials
(physiology, radiation effects)
- Adult
- Aged
- Antibodies
(blood)
- Charcot-Marie-Tooth Disease
(physiopathology)
- Electromyography
- Female
- Humans
- Male
- Median Nerve
(physiopathology)
- Middle Aged
- Myelin-Associated Glycoprotein
(immunology)
- Neural Conduction
(physiology)
- Peripheral Nervous System Diseases
(immunology, physiopathology)
- Reaction Time
(physiology)
- Ulnar Nerve
(physiopathology)
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