From: How to spot ocular abnormalities in progressive supranuclear palsy? A practical review
Aetiology | Disorders |
---|---|
• Neurodegenerative |  • Progressive supranuclear palsy (PSP) |
 • Dementia with Lewy body (DLB) | |
 • Corticobasal degeneration (CBD) | |
 • Frontotemporal dementia (FTD) | |
 • Alzheimer’s disease (AD) | |
• Heredodegenerative |  • Kufor Rakeb disease |
 • Niemann-Pick disease, type C | |
 • Perry syndrome | |
 • Mitochondrial disease (POLG) | |
 • Dentatorubral pallidoluysian atrophy | |
 • Gaucher disease | |
 • Huntington’s disease | |
 • Wilson’s disease | |
 • Neuroacanthocytosis | |
• Vascular |  • Vascular-Progressive supranuclear palsy (Vascular-PSP) |
 • Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) | |
• Infection |  • Neurosyphilis |
 • Whipple’s disease | |
• Prion |  • Prion’s disease |
• Immune-mediated |  • Paraneoplastic encephalitis (Anti-Ma1, Anti-Ma2 antibodies) |