Specific disturbances of LD movement or tethering have been linked to congenital disorders of autophagy, including SNX14‐related spinocerebellar ataxia, BICD2‐related spinal muscular atrophy, and several forms of hereditary spastic paraplegia including SPG3A/ATL1, SPG4/SPAST, SPG11/KIAA1840, and SPG20/SPART.27 This evidence concerns the gene SPG11 and proximal spinal muscular atrophy.