Autosomal dominant centronuclear myopathy

An inherited neuromuscular disorder defined by numerous centrally placed nuclei on muscle biopsy and clinical features of a congenital myopathy.

Also known as: AD-CNM, CNM1, autosomal dominant centronuclear myopathy, autosomal dominant centronuclear myopathy caused by mutation in MYF6, centronuclear myopathy 1, centronuclear myopathy, autosomal dominant, centronuclear myopathy, autosomal, modifier of, myopathy, centronuclear, 1

37 clinical trials for this condition and its sub-types.