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Published on: July 9, 2014
[Guillain-Barre syndrome: a study of 13 children]
A Roca González1, A Palomeque Rico, X Pastor Durán
1Servicio de Pediatría, Hospital Clinic, Barcelona.
Insights
This study analyzed 13 children with Guillain-Barré syndrome, finding infectious illness preceded symptoms in most. Corticosteroid treatment did not alter outcomes in this pediatric Guillain-Barré syndrome cohort.
Area of Science:
- Pediatric Neurology
- Infectious Diseases
- Immunology
Context:
- Guillain-Barré syndrome (GBS) is an autoimmune disorder affecting the peripheral nervous system.
- Pediatric GBS presents unique challenges in diagnosis and management.
- Understanding GBS in children is crucial for effective treatment strategies.
Purpose:
- To retrospectively analyze the clinical features and outcomes of pediatric Guillain-Barré syndrome.
- To identify potential triggers and associated conditions in children with GBS.
- To evaluate the impact of corticosteroid treatment on GBS outcomes in children.
Summary:
- Thirteen children (aged 2-14 years) diagnosed with Guillain-Barré syndrome were studied.
- Preceding infectious illness was noted in 75% of cases, with specific agents identified in four.
- Common symptoms included limb motor deficits, absent reflexes, cranial nerve involvement (46%), and meningitic signs (62%). One patient had Fisher syndrome variant; two required ventilation.
- Associated immunologic abnormalities were present in three children, including selective IgA deficiency, elevated IgE, and Kawasaki syndrome.
Impact:
- This research highlights the diverse clinical presentations of pediatric Guillain-Barré syndrome.
- Findings suggest infectious triggers are common in childhood GBS.
- The study provides insights into the management and outcomes of GBS in a pediatric population, noting no significant difference with corticosteroid use in this cohort.
Abstract:
A group of 13 children, aged 2 to 14 years, and diagnosed with Guillain-Barré syndrome has been analyzed. Clinical features and outcome were retrospectively studied. In 75% of the patients there was an infectious illness previous to the neurologic symptoms and in four children the etiologic agent was demonstrated. Motor deficits affecting the limbs and muscle stretch reflexes were absent in all thirteen patients. Cranial nerve involvement showed-up in 46%. Meningitic symptoms occurred in 62% of the cases. One of the children developed the Fisher syndrome variant. Two patients required assisted ventilation. Three children showed associated immunologic abnormalities, with one of the patients having a selective IgA deficiency, another child showing an increment in IgE and the other Kawasaki syndrome. We have not demonstrated differences in the outcome between the patients with corticoid treatment.
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