“…3E), CDSMA (congenital and sometimes accompanied by arthrogryposis), SPSMA (scapulopeoneal muscular atrophy), CMT2C (muscle weakness and sensory involvement) and dHMN (length-dependent condition and no sensory involvement) separately. Furthermore, a literature review of the clinical characteristics of CMT2C patients [3,4,7,[10][11][12][13][14][15][16][17] (Table 1) and SPSMA [3,9,13,[18][19][20][21] were performed (Table e-1). In the summary table, we showed that CMT2C might also have other manifestations in addition to nervous system involvement, such as vocal cord paralysis (37/48, 77%), hearing loss (12/42, 29%), and scoliosis (10/37, 27%).…”