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10th International Conference on Neurological disorders & Stroke

Paris, France

Gabriel Alejandro B. Baroque

University of Santo Tomas Hospital,Philippines

Title: Multifocal Motor Neuropathy: A Case Report


Biography: Gabriel Alejandro B. Baroque


We report a case of a 51-year old Filipino female with multifocal motor neuropathy who presented with chronic weakness of the left foot which without any sensory deficits.

With the history chronic progressive weakness, lack of sensory deficits, confirmatory by biochemical workups and diagnostics: an elevated ganglioside GM1 antibody test which revealed a titer of 1:12800, electromyography and nerve conduction confirmed the diagnosis of multifocal motor neuropathy.

Treatment of intravenous immunoglobulin with a  dose of 2g/kg over 2-5 days was initiated and repeated every 2 months with noticeable improvement.

Multifocal motor neuropathy is a rare disorder which has a prevalence of 0.6 per 100,000 individuals. It is seen in more in males with a ratio of 2.7:1. It is described as a pure motor disease without sensory deficits which is predominantly seen in the upper extremities.7 The diagnosis for the disorder is supported by determination of ganglioside GM1 antibodies, electromyography and nerve conduction velocity study (EMG-NCV).2,3,4,5