Other significant clinical clues in demyelinating CMT subtypes included vocal cord paralysis in GDAP1, ophtalmoparesis and tongue fasciculations in FGD4, severe sensory ataxia in PRX, respiratory involvement in MTMR2 and SBF2, similar to previous reports [31, 33, 34, 35]. The gene discussed is GDAP1; the disease is Vocal cord paralysis.