DNM2 and autosomal dominant centronuclear myopathy: Distinct mutations in dynamin 2 have previously been associated with other phenotypes including two forms of Charcot-Marie-Tooth disease: axonal CMT2M (MIM# 606482) originally reported by Züchner et al. [12] and intermediate form CMTDIB (MIM# 606482) reported by Kennerson et al. [13]; centronuclear myopathy ADCNM (MIM# 160150) originally reported by Bitoun et al. [14], and lethal congenital contractures syndrome type 5 LCCS5 (MIM#615368).