The study aims to gather and analyze data on patients with myasthenia gravis in France.
Utilized a national registry to collect data on patients with confirmed diagnosis of myasthenia gravis.
Analyzed characteristics and management of these patients across various healthcare settings.
Identified a significant number of myasthenia gravis patients not managed in reference centres.
Provided reference data to better understand the patient population in France.
Abstract
This national registry study provides reference data for patients in France with a confirmed diagnosis of MG. However, all patients with MG are still not managed in dedicated reference centres.