Congenital myopathies in adults: A diagnosis not to overlook.
Maria João PintoBárbara Alves PassosAna GrangeiaJoana GuimarãesLuís BrazPublished in: Acta neurologica Scandinavica (2022)
In our cohort, the majority of CM were diagnosed in adulthood, despite most having pediatric-onset symptoms and positive family history. The diagnostic delay may be associated with mild presentation, slow course, atypical muscle histology, and lack of awareness of adult-onset CM. Studies with larger populations are needed.