Centronuclear myopathy (CNM) is an inherited neuromuscular disorder characterised by clinical features of a congenital myopathy and centrally placed nuclei on muscle biopsy. It encompasses the X-linked form, the autosomal recessive form and the autosomal dominant form with a highly variable clinical presentation.
Also indexed as
Autosomal dominant centronuclear myopathyAutosomal recessive centronuclear myopathyCentronuclear myopathyCentronuclear myopathy with type I fibre hypotrophyMyotubular myopathySevere infantile myotubular myopathymyotubular centronuclear myopathysevere x-linked myotubular myopathyx-linked centronuclear myopathy
Nearby in Congenital myopathy with structural abnormalities