# A Case Report of Guillain-Barré Syndrome Presenting as Facial Diplegia: A Deviation From the Classical Ascending Paralysis

**Authors:** Syed Abubacker, Yosif Albrahem, Hannah Shaw, Suhad Jalodi, Vikneswaran Raj Nagarajan, Asim Khaleeq, Syed Jafri

PMC · DOI: 10.7759/cureus.101786 · Cureus · 2026-01-18

## TL;DR

This case report describes a rare instance of Guillain-Barré Syndrome (GBS) initially presenting as facial diplegia, not the usual ascending paralysis.

## Contribution

The paper presents a rare clinical case of GBS with an atypical initial presentation of facial diplegia.

## Key findings

- GBS can rarely present with bilateral facial nerve palsy as the initial symptom.
- Bilateral lower motor neuron facial palsy should raise suspicion for secondary causes like GBS.
- The case emphasizes the need for thorough evaluation in atypical presentations of facial palsy.

## Abstract

Guillain-Barré syndrome (GBS) is an immune-mediated inflammatory disorder affecting the peripheral nerves, typically presenting with ascending paralysis and areflexia in the lower limbs, but can also have other variable presentations. Such variable presentations can rarely include an isolated involvement of the facial nerve as the initial presenting feature. We explore a case of a 53-year-old male patient who initially came with bilateral lower motor neuron facial nerve palsy, preliminarily diagnosed as inflammatory Bell’s palsy. However, the patient later re-presented with further neurological deficits involving the lower limbs, prompting further investigations that subsequently led to the diagnosis of GBS. This case highlights the importance of having a high index of suspicion for GBS when evaluating patients presenting solely with bilateral lower motor neuron facial nerve palsy, as GBS can rarely present in such a manner. While Bell’s palsy remains a common cause of facial palsy, bilateral involvement is unusual and should prompt evaluation for secondary causes such as GBS.

## Linked entities

- **Diseases:** Guillain-Barré Syndrome (MONDO:0016218), Bell’s palsy (MONDO:0005665)

## Full-text entities

- **Genes:** ACE (angiotensin I converting enzyme) [NCBI Gene 1636] {aka ACE1, CD143, DCP, DCP1}, MUSK (muscle associated receptor tyrosine kinase) [NCBI Gene 4593] {aka CMS9, FADS}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, AP2B1 (adaptor related protein complex 2 subunit beta 1) [NCBI Gene 163] {aka ADTB2, AP105B, AP2-BETA, CLAPB1}
- **Diseases:** leg pain (MESH:D010146), flu (MESH:D007251), earache (MESH:D004433), facial nerve involvement (MESH:D020220), trauma (MESH:D014947), gastrointestinal or respiratory infection (MESH:D012141), headache (MESH:D006261), inflammation (MESH:D007249), Diplegia (MESH:D002547), Lyme disease (MESH:D008193), Venereal Disease (MESH:D012749), facial weakness (MESH:D018908), GBS (MESH:D020275), Paralysis (MESH:D010243), ascending paralysis (MESH:C537217), autoimmune (MESH:D001327), Bell's palsy (MESH:D020330), respiratory muscle paralysis (MESH:D012133), neurological deficits (MESH:D009461), vertebrae (MESH:C562952), fever (MESH:D005334), demyelinating (MESH:D003711), facial nerve palsies (MESH:D005155), respiratory or gastrointestinal symptoms (MESH:D012818), numbness (MESH:D006987), facial diplegia (MESH:C531747), infections (MESH:D007239), sarcoidosis (MESH:D012507), COVID-19 (MESH:D000086382), loss of taste (MESH:D000370), areflexia (MESH:D000071699), facial palsy (MESH:D005158), HIV (MESH:D015658)
- **Chemicals:** acetylcholine (MESH:D000109), valaciclovir (MESH:D000077483), glycolipid (MESH:D006017), LOS (MESH:C023023), amitriptyline (MESH:D000639), steroids (MESH:D013256)
- **Species:** Borreliella burgdorferi (Lyme disease spirochete, species) [taxon 139], Human immunodeficiency virus 1 (no rank) [taxon 11676], Homo sapiens (human, species) [taxon 9606], Treponema pallidum (species) [taxon 160]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12911957/full.md

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12911957/full.md

## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC12911957/full.md

---
Source: https://tomesphere.com/paper/PMC12911957