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Bumbling, Stumbling, Fumbling: Weakness, Steppage Gait, and Facial Droop in a 3-Year-Old Male
Aviva J Whelan1, Abdullah Tolaymat1, Shane C Rainey1
1University of Illinois College of Medicine at Peoria, Peoria, IL, USA.
Insights
Guillain-Barré syndrome (GBS) can present nonclassically in children with facial droop and limb pain following respiratory illness. Early diagnosis and treatment with intravenous immunoglobulin (IVIG) are crucial for recovery.
Area of Science:
- Pediatric Neurology
- Infectious Diseases
- Immunology
Background:
- Childhood weakness and gait disturbances pose diagnostic challenges.
- Guillain-Barré syndrome (GBS) is a leading cause of acute paralysis in children.
- Atypical presentations of GBS can mimic other neurological conditions.
Purpose of the Study:
- To highlight a case of GBS presenting with facial palsy and limb pain in a child.
- To emphasize the importance of considering GBS in the differential diagnosis of pediatric gait disturbances.
- To illustrate the diagnostic process and management of GBS in a pediatric patient.
Main Methods:
- Case report of a previously healthy, unimmunized 3-year-old boy.
- Clinical examination revealing facial nerve palsy, lower extremity pain, and areflexia.
- Diagnostic workup including MRI, cerebrospinal fluid (CSF) analysis, and serological testing for Mycoplasma.
- Treatment initiated with intravenous immunoglobulin (IVIG) for presumed GBS and Mycoplasma infection.
Main Results:
- The patient presented with right facial droop, clumsiness, and bilateral hip pain after a brief febrile illness.
- Cerebrospinal fluid (CSF) analysis showed elevated protein and albumin.
- Serum Mycoplasma IgM and IgG were elevated, suggesting a recent infection.
- The clinical presentation and investigations were highly suggestive of Guillain-Barré syndrome (GBS).
Conclusions:
- Gait disturbance and weakness in children warrant a thorough neurological evaluation.
- Mycoplasma infection can be an antecedent trigger for GBS.
- Prompt recognition and immunotherapy, such as IVIG, are vital for managing GBS and preventing complications like respiratory failure.
Abstract:
A previously healthy, unimmunized, 3-year-old Caucasian boy presented to the emergency department with right-sided facial droop, clumsiness, and intermittent bilateral hip pain. Two weeks ago, he had 24 hours of self-resolving rhinorrhea and fever. Examination was significant for right facial nerve palsy, lower extremity pain, areflexia of his right lower extremity, and diminished reflexes of his left lower extremity. He was admitted for urgent magnetic resonance imaging of the brain. Cerebrospinal fluid (CSF) protein was 85 mg/dL with elevated albumin and immunoglobulin, and CSF white blood cell was 3 cells/mm3. Serum Mycoplasma immunoglobulin (Ig) M and IgG were elevated. There was concern for Guillain-Barré syndrome (GBS). He was started on intravenous IG (IVIG) and was treated for presumed Mycoplasma infection. Weakness and gait disturbances in a child can present the clinician with a diagnostic challenge. Gait disturbance may indicate a neurological lesion anywhere from the central nervous system to the peripheral nerves, neuromuscular junction, or muscle. In the present case, the combination of peripheral facial palsy, presumed neuropathic pain, gait difficulties, and areflexia in the setting of an antecedent respiratory illness were suggestive of GBS. The cornerstone treatments involve hospitalization to facilitate continuous monitoring for serious sequelae, such as acute respiratory failure and cardiac dysrhythmia, followed by immunotherapy with IVIG or plasma exchange. Gait disturbance and weakness in a child is a diagnostic challenge. GBS is the most common cause of acute paralysis in the Western world and should remain high on the clinician's differential diagnosis. However, patients with GBS may also present nonclassically with extremity pain and cranial nerve palsies.
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