ABSTRACT
Multifocal motor neuropathy (MMN) with conduction block is an acquired, autoimmune-mediated
neuropathy that is responsive to treatment. The clinical history is one of slowly,
progressive distal weakness, which more commonly involves the upper extremities, and
it affects mainly young adults. Physical examination reveals weakness without sensory
loss in the distribution of individual nerves. Atrophy may be present, but hyperreflexia
and spasticity are not seen. Electrophysiological studies reveal motor conduction
blocks at sites not prone to compression with normal sensory responses. Immunoglobulin
M anti-GM1 titers may be elevated. Treatment with human immunoglobulin or cyclophosphamide
has been shown to improve strength in the majority of patients with MMN in the short
term. However, motor strength and function may gradually decline over years in spite
of long-term therapy.
KEYWORDS
Multifocal motor neuropathy with conduction block - diagnosis - treatment