FHL1 and Emery-Dreifuss muscular dystrophy: Mutations in the structure of four-and-a-half LIM domains 1 (FHL1) gene have been described in the last decade to be associated with a large spectrum of diseases, including Emery-Dreifuss muscular dystrophy (EDMD); X-linked scapuloperoneal myopathy (X-SPM); reducing bodies myopathies (RBM); X-linked myopathy with postural muscle atrophy (X-MPMA); rigid spine syndrome and more rarely HCM [2].