disease 2,994 words KG: ent-dise-4fb6cf36
Contents

Autonomic Dysfunction in Corticobasal Syndrome

Disease Info
Typical OnsetMSA often has earlier autonomic involvement
Orthostatic hypotension30-50% of patients
Urinary dysfunctionUrinary urgency and frequency, but less severe than in MSA
Gastrointestinal dysfunctionConstipation is common; dysphagia can occur
Sexual dysfunction30-40% of male patients
Sweating abnormalitiesHyperhidrosis or hypohidrosis
Urinary symptoms40-60% of patients
Constipation50-70% of patients
Sweating changes20-30% of patients
ProgressionMSA has more rapid progression
SeverityMSA has more severe autonomic failure
ImpactCan significantly affect quality of life
DatabasesOMIMOrphanetClinicalTrialsPubMed

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Related Hypotheses (12)

Multi-Modal Stress Response Harmonization
Score: 0.76
Circadian-Synchronized Proteostasis Enhancement
Score: 0.74
Aquaporin-4 Polarization Rescue
Score: 0.73
Noradrenergic-Tau Propagation Blockade
Score: 0.71
Microglial Purinergic Reprogramming
Score: 0.70
Glial Glycocalyx Remodeling Therapy
Score: 0.65
Ephrin-B2/EphB4 Axis Manipulation
Score: 0.64
Vagal Afferent Microbial Signal Modulation
Score: 0.62
Sphingolipid Metabolism Reprogramming
Score: 0.62
Synaptic Vesicle Tau Capture Inhibition
Score: 0.58
Trans-Synaptic Adhesion Molecule Modulation
Score: 0.54
Enteric Nervous System Prion-Like Propagation Blockade
Score: 0.48

Related Analyses (11)

Metabolic reprogramming in neurodegenerative disease
neurodegeneration · completed
Autophagy-lysosome pathway convergence across neurodegenerat
neurodegeneration · completed
Autophagy-lysosome pathway convergence across neurodegenerat
neurodegeneration · archived
Protein aggregation cross-seeding across neurodegenerative d
neurodegeneration · completed
Lipid raft composition changes in synaptic neurodegeneration
neurodegeneration · completed

Related Experiments (1)

Cytochrome Therapeutics
clinical · proposed · Score: 0.40

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