Mutations in DYNC1H1 gene could cause spinal muscular atrophy, intellectual disability, frontotemporal dementia and Parkinson’s disease (Willemsen et al., 2012; Szczałuba et al., 2018; Maretina et al., 2019; Mentis et al., 2021). The gene discussed is DYNC1H1; the disease is frontotemporal dementia.