Data availability
Not applicable.
References
Gabrych DR, Lau VZ, Niwa S, Silverman MA (2019) Going too far is the same as falling short†: kinesin-3 family members in hereditary spastic paraplegia. Front Cell Neurosci 26(13):419
Caballero Oteyza A, Battaloğlu E, Ocek L, Lindig T, Reichbauer J, Rebelo AP et al (2014) Motor protein mutations cause a new form of hereditary spastic paraplegia. Neurology 82(22):2007–2016
Marchionni E, Méneret A, Keren B, Melki J, Denier C, Durr A et al (2019) KIF1C variants are associated with hypomyelination, ataxia, tremor, and dystonia in fraternal twins. Tremor Other Hyperkinet Mov (NY) 17:9
Dor T, Cinnamon Y, Raymond L, Shaag A, Bouslam N, Bouhouche A et al (2014) KIF1C mutations in two families with hereditary spastic paraparesis and cerebellar dysfunction. J Med Genet 51(2):137–142
Yücel-Yılmaz D, Yücesan E, Yalnızoğlu D, Oğuz KK, Sağıroğlu MŞ, Özbek U et al (2018) Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span. Brain Dev 40(6):458–464
Funding
Not applicable.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Conflict of interest
The author declares no conflict of interest.
Informed consent
Available.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
About this article
Cite this article
Mahale, R., Padmanabha, H., Mailankody, P. et al. Late-onset spastic-ataxia due to KIF1C mutation: broadening the SPG 58 phenotype. Acta Neurol Belg (2023). https://doi.org/10.1007/s13760-023-02437-1
Received:
Accepted:
Published:
DOI: https://doi.org/10.1007/s13760-023-02437-1