Multifocal motor neuropathy. Immediate response to intravenous immunoglobulin
Multifocal motor neuropathy, a rare insidious immune-mediated disorder, features muscular weakness and atrophy, as well as arreflexia, due to nerve conduction block and is often associated with the presence of anti-GM1antibody. We report a patient with a nine-year history of progressive upper limb w...
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2001
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Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00257680_v61_n4_p441_Cammarota http://hdl.handle.net/20.500.12110/paper_00257680_v61_n4_p441_Cammarota |
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paper:paper_00257680_v61_n4_p441_Cammarota2023-06-08T14:53:34Z Multifocal motor neuropathy. Immediate response to intravenous immunoglobulin Immunoglobulin Multifocal motor neuropathy immunoglobulin immunoglobulin adult amyotrophic lateral sclerosis article case report clinical feature diagnostic error disease course human male motoneuron motor neuropathy muscle strength nerve block treatment outcome amyotrophic lateral sclerosis differential diagnosis middle aged motor neuron disease nerve conduction Amyotrophic Lateral Sclerosis Diagnosis, Differential Humans Immunoglobulins, Intravenous Male Middle Aged Motor Neuron Disease Neural Conduction Multifocal motor neuropathy, a rare insidious immune-mediated disorder, features muscular weakness and atrophy, as well as arreflexia, due to nerve conduction block and is often associated with the presence of anti-GM1antibody. We report a patient with a nine-year history of progressive upper limb weakness, misdiagnosed as amyotrophic lateral sclerosis, who responded within hours to intravenous immunoglobulin treatment with full recovery of muscle strength. This case highlights the need to search for conduction block in patients with lower motor neuron involvement. 2001 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00257680_v61_n4_p441_Cammarota http://hdl.handle.net/20.500.12110/paper_00257680_v61_n4_p441_Cammarota |
institution |
Universidad de Buenos Aires |
institution_str |
I-28 |
repository_str |
R-134 |
collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
topic |
Immunoglobulin Multifocal motor neuropathy immunoglobulin immunoglobulin adult amyotrophic lateral sclerosis article case report clinical feature diagnostic error disease course human male motoneuron motor neuropathy muscle strength nerve block treatment outcome amyotrophic lateral sclerosis differential diagnosis middle aged motor neuron disease nerve conduction Amyotrophic Lateral Sclerosis Diagnosis, Differential Humans Immunoglobulins, Intravenous Male Middle Aged Motor Neuron Disease Neural Conduction |
spellingShingle |
Immunoglobulin Multifocal motor neuropathy immunoglobulin immunoglobulin adult amyotrophic lateral sclerosis article case report clinical feature diagnostic error disease course human male motoneuron motor neuropathy muscle strength nerve block treatment outcome amyotrophic lateral sclerosis differential diagnosis middle aged motor neuron disease nerve conduction Amyotrophic Lateral Sclerosis Diagnosis, Differential Humans Immunoglobulins, Intravenous Male Middle Aged Motor Neuron Disease Neural Conduction Multifocal motor neuropathy. Immediate response to intravenous immunoglobulin |
topic_facet |
Immunoglobulin Multifocal motor neuropathy immunoglobulin immunoglobulin adult amyotrophic lateral sclerosis article case report clinical feature diagnostic error disease course human male motoneuron motor neuropathy muscle strength nerve block treatment outcome amyotrophic lateral sclerosis differential diagnosis middle aged motor neuron disease nerve conduction Amyotrophic Lateral Sclerosis Diagnosis, Differential Humans Immunoglobulins, Intravenous Male Middle Aged Motor Neuron Disease Neural Conduction |
description |
Multifocal motor neuropathy, a rare insidious immune-mediated disorder, features muscular weakness and atrophy, as well as arreflexia, due to nerve conduction block and is often associated with the presence of anti-GM1antibody. We report a patient with a nine-year history of progressive upper limb weakness, misdiagnosed as amyotrophic lateral sclerosis, who responded within hours to intravenous immunoglobulin treatment with full recovery of muscle strength. This case highlights the need to search for conduction block in patients with lower motor neuron involvement. |
title |
Multifocal motor neuropathy. Immediate response to intravenous immunoglobulin |
title_short |
Multifocal motor neuropathy. Immediate response to intravenous immunoglobulin |
title_full |
Multifocal motor neuropathy. Immediate response to intravenous immunoglobulin |
title_fullStr |
Multifocal motor neuropathy. Immediate response to intravenous immunoglobulin |
title_full_unstemmed |
Multifocal motor neuropathy. Immediate response to intravenous immunoglobulin |
title_sort |
multifocal motor neuropathy. immediate response to intravenous immunoglobulin |
publishDate |
2001 |
url |
https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00257680_v61_n4_p441_Cammarota http://hdl.handle.net/20.500.12110/paper_00257680_v61_n4_p441_Cammarota |
_version_ |
1768543883789074432 |