Clinical, biological, electrophysiological and therapeutic profile of patients with anti-MAG neuropathy according to MYD88 L265P and CXCR4 mutations and underlying haemopathy.
Alexandre GuérémyJosé BoucrautJohn BoudjaraneAude-Marie GrapperonEtienne FortanierLaure FarnaultJean GabertFrédéric VelyRomaric LacroixLudivine KoutonShahram AttarianEmilien DelmontPublished in: Journal of neurology (2023)
mutation and underlying haemopathies are not predictive of a more severe disease. However, in cases of resistant and progressive neuropathy, they provide an opportunity to prescribe newly available drugs such as Bruton tyrosine kinase inhibitors.