Mapping Anatomical Cerebellar Changes and their Neurocognitive Manifestations in SCA34: A Detailed Case Analysis
Spinocerebellar Ataxia Type 34 is a rare hereditary ataxia characterised by progressive cerebellar degeneration, motor impairment, and dermatological features, with cognitive manifestations remaining poorly understood. This case report presents neurocognitive and neuroimaging profiles of two Swedish male patients with genetically confirmed SCA34. Both underwent an extensive neuropsychological test
