| Literature DB >> 12486564 |
D Fischer1, J Reimann, R Schröder, St Schmidt.
Abstract
Multifocal motor neuropathy (MMN) is an acquired immune mediated motor neuropathy with characteristic clinical and neurographic features.Clinically, MMN is characterized by progressive, predominantly distal and asymmetrical limb weakness. Neurographic recordings demonstrate features of multifocal demyelination with or without conduction block. Sensory nerves are not affected. Due to strict diagnostic criteria,MMN may be underdiagnosed in patients with motor neuropathies. Since intravenous immunglobulins are an efficient therapy for MMN,clinical and electrophysiological differentiation from other neuromuscular disorders is mandatory to prevent progressive impairment of motor function. We present a patient with MMN and review the clinical, electrophysiological, and histological features. In addition,pathogenesis, differential diagnosis and treatment of MMN are discussed.Entities:
Mesh:
Year: 2002 PMID: 12486564 DOI: 10.1007/s00115-002-1440-y
Source DB: PubMed Journal: Nervenarzt ISSN: 0028-2804 Impact factor: 1.214