DNM2 and hereditary spastic paraplegia: Autosomal‐dominant centronuclear myopathy results from mutations in the DNM2 gene which encodes Dynamin 2 (DNM2) (Bitoun et al, 2005) also involved in rare cases of Charcot–Marie–Tooth disease (Zuchner et al, 2005) and hereditary spastic paraplegia (Sambuughin et al, 2015).