TTR and amyloidosis: Similar neuropathological findings, previously labelled as oculoleptomeningeal amyloidosis, have also been also described in single‐case reports of patients with other TTR mutations, such as Asp18Gly, Ala25Thr, Val30Gly, Tyr69His, Tyr114Cys, and Gly47Arg,86, 87, 88 suggesting that the CNS involvement in hATTR is not specific to a few mutations.