Pharyngeal-cervical-brachial variant of Guillain-Barré syndrome
Synonyms: PCB variant of GBS · PCB variant of Guillain-Barré syndrome · Pharyngeal-cervical-brachial weakness · Pharyngo-cervico-brachial variant of GBS · Pharyngo-cervico-brachial variant of Guillain-Barré syndrome
- Type
- Disease
- Group
- Disorder
- Inheritance
- Multigenic/multifactorial, Not applicable
- Age of onset
- All ages
- Status
- active
Pharyngeal-cervical-brachial variant of Guillain-Barré syndrome is a rare, acquired peripheral neuropathy disease characterized by rapidly progressive oropharyngeal (facial palsy, dysarthria) and cervicobrachial weakness, associated with upper limb weakness and hypo/areflexia, in the absence of ophthalmoplegia, ataxia, altered consciousness, and prominent lower limb weakness. The presence of monospecific IgG anti-GT1a antibodies is associated.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Pharyngeal-cervical-brachial variant of Guillain-Barré syndrome | PCB variant of GBS · PCB variant of Guillain-Barré syndrome · Pharyngeal-cervical-brachial weakness · Pharyngo-cervico-brachial variant of GBS · Pharyngo-cervico-brachial variant of Guillain-Barré syndrome |
| fr | Variant pharyngo-cervico-brachial du syndrome de Guillain-Barré | Faiblesse pharyngo-cervico-brachiale · Variant PCB du SGB · Variant PCB du syndrome de Guillain-Barré · Variant pharyngo-cervico-brachial du SGB |
| de | Guillain-Barré-Syndrom, pharyngeal-zervikal-brachiale Variante | |
| es | Variante faringo-cérvico-braquial del síndrome de Guillain-Barré | |
| it | Variante faringea-cervicale-brachiale della sindrome di Guillain-Barré | |
| nl | Faryngeale-cervicale-brachiale variant van syndroom van Guillain-Barré | PCB variant van syndroom van Guillain-Barré · Faryngeale-cervicale-brachiale zwakte · Faryngo-cervico-brachiale variant van GBS · Faryngo-cervico-brachiale variant van syndroom van Guillain-Barré · PCB variant van GBS |
| pt | Variante faringea-cervical-braqueal da síndrome de Guillain-Barré | |
| pl | Gardłowo-szyjno-ramienny wariant zespołu Guillaina i Barrégo | Gardłowo-szyjno-ramienny wariant GBS · Gardłowo-szyjno-ramienny wariant zespołu Guillaina i Barrégo · PCB wariant GBS · PCB wariant zespołu Guillaina i Barrégo · Słabość gardłowo-szyjno-ramienna |
| cs | Faryngo-cerviko-brachiální varianta Guillainova-Barrého syndromu | PCB varianta GBS · PCB varianta Guillainova-Barrého syndromu · Faryngo-cerviko-brachiální varianta Guillain-Barrého syndromu · Faryngo-cerviko-brachiální slabost · Faryngo-cerviko-brachiální varianta GBS · PCB varianta Guillain-Barrého syndromu |
| uk | Глотково-шийно-плечовий варіант синдрому Гійєна-Барре | Варіант друкованої плати GBS · ПХБ-варіант синдрому Гійєна-Барре · Глотково-шийно-плечова слабкість · Фаринго-цервіко-брахіальний варіант GBS · Фаринго-цервіко-брахіальний варіант синдрому Гійєна-Барре |
| zh | 吉兰-巴雷综合征咽-颈-臂变体 | 吉兰-巴雷综合征咽-颈-臂变体 |
| tr | Guillain-Barrè sendromunun faringeal-servikal-brakiyal varyantı | GBS'nin PCB varyantı · Faringeal-servikal-brakiyal zayıflık · Guillain-Barré sendromunun PCB varyantı · GBS'nin faringo-serviko-brakiyal varyantı · Guillain-Barré sendromunun faringo-serviko-brakiyal varyantı |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | G61.0 | NTBT | attributed | validated |
| ICD-11 | 8C01.0 | NTBT | index | validated |
| MONDO | 0016496 | E | validated | |
| UMLS | C5190783 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:231416Regional variant of Guillain-Barré syndrome
rare neurological diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/231426
- This record as JSON: /data/d/231426.json