HSPB8 and distal myopathy: Heat shock protein HSPB8 also known as HSP22 (22 kDa) is a cytoplasmic protein that serves as a member of the chaperone‐assisted autophagy complex and is involved in Charcot‐Marie‐Tooth disease type 2L as well as in a rare form of human distal myopathy (Ghaoui et al., 2016).