Kisho is an information platform, not a medical provider. Nothing on this site constitutes medical advice, diagnosis, or treatment recommendations. All content is aggregated from publicly available sources (including ClinicalTrials.gov, PubMed, FDA.gov, and Orphanet) and is provided for informational purposes only. Clinical trial eligibility, treatment decisions, and any health-related actions should always be discussed with a qualified healthcare professional. Kisho does not endorse any specific therapy, organization, or clinical trial. Terms of use · Privacy policy
Acute sensory ataxic neuropathy is a rare variant of Guillain-Barré syndrome characterized by acute onset monophasic sensory neuropathy with diminished or absent tendon reflexes, loss of proprioception, positive Romberg sign and nerve conduction features of demyelination. It presents several weeks after acute infection with paresthesias, ataxia and neuropathic pain.
No clinical trials have been registered for acute sensory ataxic neuropathy.
5 publications have been identified in PubMed for acute sensory ataxic neuropathy. Research spans Review / Meta-Analysis (40%), Case Report / Case Series (40%), and Other (20%).
Bannai T (2026). [PMID: 41598737](https://pubmed.ncbi.nlm.nih.gov/41598737/). *Journal of clinical medicine*. [Case Report / Case Series]
Kinoshita T (2026). [PMID: 41717799](https://pubmed.ncbi.nlm.nih.gov/41717799/). *Physiotherapy theory and practice*. [Case Report / Case Series]
Siow SF (2024). [PMID: 38978727](https://pubmed.ncbi.nlm.nih.gov/38978727/). *Brain communications*. [Other]
Pascual-Goñi E (2024). [PMID: 39088795](https://pubmed.ncbi.nlm.nih.gov/39088795/). *Neurology*. [Review / Meta-Analysis]
Lee SU (2024). [PMID: 38739407](https://pubmed.ncbi.nlm.nih.gov/38739407/). *JAMA neurology*. [Review / Meta-Analysis]
Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 4:32 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center
Common questions about acute sensory ataxic neuropathy