Motor Neuron Involvement in Two ATP13A2-Related Families: ALS And HSP-Like Phenotypes

Sepehr Khosravi1, Elaheh Amini1,2, Maziar Emamikhah3

  • 1Department of Neurology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.

Summary

Mutations in the ATP13A2 gene cause neurodegenerative disorders. This study details two Iranian families with ATP13A2 variants presenting atypical Kufor-Rakeb syndrome (KRS) features, expanding the known disease spectrum.