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  Vol. 63 No. 12, December 2006 TABLE OF CONTENTS
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Multifocal Motor Neuropathy With Conduction Block

Slow But Not Benign

Dale J. Lange, MD; Louis H. Weimer, MD; Werner Trojaborg, MD, DMSci; Robert E. Lovelace, MD; Clifton L. Gooch, MD; Lewis P. Rowland, MD

Arch Neurol. 2006;63:1778-1781.

Objective  To describe a patient with multifocal motor neuropathy with conduction block who had annual clinical and physiological examinations for 18 years but declined treatment for personal reasons.

Design  Case report.

Setting  Collaboration between 2 academic tertiary care hospitals.

Patient  One patient with multifocal motor neuropathy with conduction block.

Results  At age 44 years, there was weakness and wasting of the left biceps with conduction block in the left musculocutaneous and right ulnar nerves. The left median nerve was inexcitable. The right median, ulnar, and left peroneal nerves developed axonal change (loss of distal compound muscle action potential amplitude) at years 5, 12, and 13. By 2005, new weakness had appeared in 20 muscles (16 in the arms); he could not use a keyboard, button buttons, or write his name. Nerves that initially showed conduction block became inexcitable over the course of the illness.

Conclusions  Multifocal motor neuropathy with conduction block is a disease that may be "only" slowly progressive but is not always benign. Nerves showing conduction block may develop axonal change. Better markers for this disease are needed.


Author Affiliations: Department of Neurology, Mt Sinai School of Medicine (Dr Lange), and The Neurological Institute, New York Presbyterian Hospital, Columbia University College of Physicians and Surgeons (Drs Weimer, Trojaborg, Lovelace, Gooch, and Rowland), New York, NY.



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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Review: Pathogenesis and treatment of immune-mediated neuropathies
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Therapeutic Advances in Neurological Disorders 2009;2:261-281.
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Multifocal motor neuropathy: review of a treatable immune mediated disorder
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Postgrad. Med. J. 2008;84:287-292.
ABSTRACT | FULL TEXT  





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