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PedAM

Pediatric Disease Annotations & Medicines




Disease polyneuropathy
Phenotype C0026470|monoclonal gammopathy of undetermined significance
Sentences 3
PubMedID- 25572169 Anti-mag neuropathy is a very rare form of acquired polyneuropathy associated with igm monoclonal gammopathy of undetermined significance (mgus).
PubMedID- 23095652 The prevalence of polyneuropathy in patients with monoclonal gammopathy of undetermined significance (mgus) has been reported to be 10-50%.
PubMedID- 22189568 In the remaining cohorts (monoclonal gammopathy of undetermined significance related polyneuropathy, multifocal motor neuropathy, mytonic dystrophy type-1, pompe's disease and limb-girdle muscular dystrophy), the muscles groups evaluated represented the clinical picture of each illness (see supplementary table 1 for available muscles per cohort).

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