raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:231450

Acute pure sensory neuropathy

Synonyms: Acute pure sensory GBS · Acute pure sensory Guillain-Barré syndrome

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

A rare, acquired, demyelinating neuropathy disease characterized by acute, symmetric, monophasic sensory neuropathy without motor involvement, typically manifesting with numbness in the distal lower limbs which progressively extends to all the limb, tingling sensation in the distal lower limbs, generalized areflexia, and unsteady gait, as well as clumsiness of the upper limbs, pseudoathetosis and loss of vibration sense.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enAcute pure sensory neuropathyAcute pure sensory GBS · Acute pure sensory Guillain-Barré syndrome
frNeuropathie sensorielle pure aiguëSGB sensoriel pur aigu · Syndrome de Guillain-Barré sensoriel pur aigu
deNeuronopathie, akute reine sensorischeGuillain-Barré-Syndrom, akutes reines sensorisches
esNeuropatía sensitiva pura agudaGBS sensitivo puro agudo · Síndrome de Guillain-Barré sensitivo puro agudo
itNeuropatia sensoriale acuta puraGBS sensoriale pura acuta · Sindrome di Guillain-Barré sensoriale pura acuta
nlAcute zuivere sensorische neuropathieAcuut zuiver sensorisch GBS · Acuut zuiver sensorisch syndroom van Guillain-Barré
ptNeuropatia sensitiva pura agudaGBS sensitiva pura aguda · Síndrome Guillain-Barré sensitiva pura aguda
plOstra izolowana neuropatia czuciowaOstry czysty czuciowy GBS · Ostry czysty czuciowy zespół Guillaina i Barrégo
csAkutní čistá sensorická neuropatieAkutní čistý sensorický GBS · Akutní čistý sensorický Guillainův-Barrého syndrom · Akutní čistý sensorický Guillain-Barrého syndrom
ukГостра ізольована сенсорна нейропатіяГострий чисто сенсорний GBS · Гострий чисто сенсорний синдром Гійєна-Барре
zh急性纯感觉神经病急性纯感觉性吉兰-巴雷综合征
trAkut saf duyusal nöropatiAkut saf duyusal GBS · Akut saf duyusal Guillain-Barré sendromu

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10G61.0NTBTattributedvalidated
MONDO0016498Evalidated
UMLSC5190881Evalidated

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

3

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