Expanding the histopathological spectrum of CFL2-related myopathies.
Fabiana FattoriC FiorilloC RodolicoG TascaM VerardoE BellacchioS PizziA CiolfiG FagiolariA LupicaP BrodaM PedemonteM MoggioC BrunoTartaglia MarcoE BertiniA D'AmicoPublished in: Clinical genetics (2018)
Congenital myopathies (CMs) caused by mutation in cofilin-2 gene (CFL2) show phenotypic heterogeneity ranging from early-onset and rapid progressive forms to milder myopathy. Muscle histology is also heterogeneous showing rods and/or myofibrillar changes. Here, we report on three new cases, from two unrelated families, of severe CM related to novel homozygous or compound heterozygous loss-of-function mutations in CFL2. Peculiar histopathological changes showed nemaline bodies and thin filaments accumulations together to myofibrillar changes, which were evocative of the muscle findings observed in Cfl2-/- knockout mouse model.