# Hypokalemic Periodic Paralysis: A Case Report of Acute Flaccid Quadriparesis Mimicking Guillain-Barré Syndrome

**Authors:** Lisha Michel M, Kiran Kumar

PMC · DOI: 10.7759/cureus.103769 · Cureus · 2026-02-17

## TL;DR

A case of hypokalemic periodic paralysis mimicking Guillain-Barré syndrome is reported, highlighting the importance of checking electrolyte levels in sudden paralysis.

## Contribution

The paper presents a rare case linking hypokalemic periodic paralysis to acute flaccid quadriparesis, emphasizing electrolyte testing for accurate diagnosis.

## Key findings

- Severe hypokalemia was identified as the cause of acute flaccid paralysis in a 30-year-old man.
- Rapid recovery occurred after potassium supplementation, distinguishing hypokalemic paralysis from Guillain-Barré syndrome.
- MRI and neurological exams failed to confirm Guillain-Barré syndrome, supporting the hypokalemic diagnosis.

## Abstract

Hypokalemic periodic paralysis (HPP) is an uncommon but reversible cause of acute flaccid paralysis. It can clinically resemble neurological emergencies such as Guillain-Barré syndrome (GBS), leading to potential misdiagnosis and delays in appropriate treatment.

We report a 30-year-old man who presented with sudden-onset quadriparesis following an acute febrile illness with gastrointestinal symptoms characterized by fever, myalgia, arthralgia, and vomiting. Initial neurological assessment demonstrated proximal and distal weakness without sensory involvement. Laboratory tests revealed severe hypokalemia (2.2 mmol/L), mild hypomagnesemia, hypophosphatemia, and markedly elevated CRP and procalcitonin. An MRI of the brain and spine was unremarkable. Although GBS was considered, rapid improvement in muscle strength following intravenous (IV) and oral potassium supplementation supported the diagnosis of hypokalemic periodic paralysis. The patient made a full recovery with the correction of electrolytes.

This case emphasizes the importance of early electrolyte evaluation in acute flaccid paralysis and highlights the need to distinguish hypokalemic paralysis from GBS, as timely potassium replacement leads to rapid and complete recovery.

## Linked entities

- **Diseases:** hypokalemic periodic paralysis (MONDO:0008223), Guillain-Barré syndrome (MONDO:0016218)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** neurological emergencies (MESH:D004630), GBS (MESH:D020275), myalgia (MESH:D063806), gastrointestinal symptoms (MESH:D012817), arthralgia (MESH:D018771), hypomagnesemia (OMIM:613882), HPP (MESH:D020514), vomiting (MESH:D014839), hypophosphatemia (MESH:D017674), flaccid paralysis (MESH:C000629404), Flaccid Quadriparesis (MESH:D011782), hypokalemia (MESH:D007008), weakness (MESH:D018908), febrile illness (MESH:D005334)
- **Chemicals:** potassium (MESH:D011188)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC13001630/full.md

## References

6 references — full list in the complete paper: https://tomesphere.com/paper/PMC13001630/full.md

---
Source: https://tomesphere.com/paper/PMC13001630