raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:231466

Acute sensory ataxic neuropathy

Synonyms: ASAN · Acute sensory ataxic GBS · Acute sensory ataxic Guillain-Barré syndrome

Type
Disease
Group
Disorder
Inheritance
Multigenic/multifactorial, Not applicable
Age of onset
All ages
Status
active

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.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enAcute sensory ataxic neuropathyASAN · Acute sensory ataxic GBS · Acute sensory ataxic Guillain-Barré syndrome
frNeuropathie ataxique sensorielle aiguëASAN · SGB ataxique sensoriel aigu · Syndrome de Guillain-Barré ataxique sensoriel aigu
deNeuropathie, akute ataxische sensorischeASAN · Guillain-Barré-Syndrom, akutes ataxische sensorisches
esNeuropatía atáxica sensitiva agudaASAN · GBS atáxico sensitivo agudo · Síndrome de Guillain-Barré atáxico sensitivo agudo
itNeuropatia atassica sensoriale acutaASAN · GBS atassica sensoriale acuta · Sindrome atassica sensoriale acuta di Guillain-Barré
nlAcute sensorische ataxische neuropathieAcuut sensorisch ataxisch syndroom van Guillain-Barré · ASAN · Acuut sensorisch ataxisch GBS
ptNeuropatia atáxica sensorial aguda
plOstra ataksja czuciowaASAN · Ostra ataksja czuciowa GBS · Ostry czuciowy ataktyczny zespół Guillaina i Barrégo
csAkutní senzorická ataxická neuropatieASAN · Akutní senzorický ataxický GBS · Akutní senzorický ataxický Guillainův-Barrého syndrom · Akutní senzorický ataxický Guillain-Barrého syndrom
ukГостра сенсорна атаксична нейропатіяГострий сенсорний атаксичний GBS · Гострий сенсорний атаксичний синдром Гійєна-Барре · ASAN
zh急性感觉共济失调性神经病急性感觉共济失调性吉兰-巴雷综合征
trAkut duyusal ataksik nöropatiASAN · Akut duyusal ataksik GBS · Akut duyusal ataksik Guillain-Barré sendromu

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10G61.0NTBTattributedvalidated
ICD-118C01.0NTBTindexvalidated
MONDO0016500Evalidated
UMLSC4707661Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

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Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card