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autoimmune autonomic ganglionopathy (AAG) - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

autoimmune autonomic ganglionopathy

MONDO:0016499

Also known as:AAGacute panautonomic GBSacute panautonomic Guillain-Barre syndrome

Overview

A rare variant of Guillain-Barré syndrome characterized by acute post-ganglionic sympathetic and parasympathetic failure presenting several weeks after acute infection with gastrointestinal symptoms (abdominal pain, vomiting, constipation, diarrhea, gastroparesis, ileus), orthostatic hypotension, erectile dysfunction, urinary frequency, urgency or retention, vasomotor instability with acrocyanosis and reduced salivation, lacrimation and sweating.

Diagnosis

Biomarker and diagnostic research for autoimmune autonomic ganglionopathy has been reported in the published literature.

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for autoimmune autonomic ganglionopathy.

17 publications have been identified in PubMed for autoimmune autonomic ganglionopathy. Research spans Case Report / Case Series (53%), Review / Meta-Analysis (24%), and Diagnostic / Biomarker (12%).

Research Type	Count	% of Total
Patient case studies	9	53%

Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 9:42 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:231457

GARD

Genetic and Rare Diseases Info Center

GARD:20617

Questions for Your Care Team

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autoimmune autonomic ganglionopathy

Overview

Diagnosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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