X-linked myotubular myopathy: A brief update Cambrón Carmona, María de los Ángeles Myotubular myopathy Centronuclear myopathy X chromosome Satellite cells MTM1 gen Myotubular Miopatía miotubular Miopatía centronuclear Cromosoma X Células satélites Miotubularina X-linked myotubular myopathy, included in the centronuclear myopathies (CNM), is a severe congenital disorder caused by mutations of the gene MTM1. With a recessive hereditary pattern linked to the X chromosome, this disorder shows a varied symptomatology and a specific histopathological pattern. The current treatment of this rare disease is still undergoing research, although gene therapy is being focalized. 2021-06-23T07:37:36Z 2021-06-23T07:37:36Z 2016 info:eu-repo/semantics/article Cambrón Carmona, María de los Ángeles. X-linked myotubular myopathy: A brief update. AMU, 4: 14-18 2341-0361 http://hdl.handle.net/10481/69343 eng http://creativecommons.org/licenses/by-nc-nd/3.0/es/ info:eu-repo/semantics/openAccess Atribución-NoComercial-SinDerivadas 3.0 España Archivos de Medicina Universitaria