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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.
Movement Disorders Clinical Practice
|March 3, 2025
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.
Area of Science:
- Genetics
- Neuroscience
- Molecular Biology
Background:
- ATP13A2 gene mutations are linked to neurodegenerative conditions like Kufor-Rakeb syndrome (KRS), neuronal ceroid lipofuscinosis (NCL), hereditary spastic paraplegia (HSP), and amyotrophic lateral sclerosis (ALS).
- This study focuses on two Iranian families with atypical KRS presentations due to ATP13A2 variants.
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