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Guillain-Barre Syndrome Presenting With Bilateral Facial Nerve Palsy

OBJECTIVE: This case study is about an 11-year-old girl with bilateral facial weakness, abnormal taste sensation, and absent deep tendon reflexes of both knees and ankles. However, the muscle power of the lower and upper extremities across all muscle groups was normal. After 2 days, she developed pa...

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Detalles Bibliográficos
Autores principales: INALOO, Sorour, KATIBEH, Pegah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shahid Beheshti University of Medical Sciences 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3943056/
https://www.ncbi.nlm.nih.gov/pubmed/24665332
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author INALOO, Sorour
KATIBEH, Pegah
author_facet INALOO, Sorour
KATIBEH, Pegah
author_sort INALOO, Sorour
collection PubMed
description OBJECTIVE: This case study is about an 11-year-old girl with bilateral facial weakness, abnormal taste sensation, and absent deep tendon reflexes of both knees and ankles. However, the muscle power of the lower and upper extremities across all muscle groups was normal. After 2 days, she developed paresthesia and numbness in the lower extremities. Other neurologic examinations, such as fundoscopic evaluation of the retina were normal with the muscle power of both upper- and lower-extremities intact. A lumbar puncture revealed albumincytological dissociation. EMG and NCV were in favor of Guillain-Barre syndrome, for which IVIG was prescribed and the abnormal sensations in the lower limbs rapidly improved. Bilateral facial diplegia without weakness and paresthesia is a variant of Guillain-Barre syndrome that mostly presents with acute onset, rapid progression with or without limb weakness, paresthesia, and decreased or absent DTR and albumin-cytological dissociation.
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spelling pubmed-39430562015-03-01 Guillain-Barre Syndrome Presenting With Bilateral Facial Nerve Palsy INALOO, Sorour KATIBEH, Pegah Iran J Child Neurol Letter to Editor OBJECTIVE: This case study is about an 11-year-old girl with bilateral facial weakness, abnormal taste sensation, and absent deep tendon reflexes of both knees and ankles. However, the muscle power of the lower and upper extremities across all muscle groups was normal. After 2 days, she developed paresthesia and numbness in the lower extremities. Other neurologic examinations, such as fundoscopic evaluation of the retina were normal with the muscle power of both upper- and lower-extremities intact. A lumbar puncture revealed albumincytological dissociation. EMG and NCV were in favor of Guillain-Barre syndrome, for which IVIG was prescribed and the abnormal sensations in the lower limbs rapidly improved. Bilateral facial diplegia without weakness and paresthesia is a variant of Guillain-Barre syndrome that mostly presents with acute onset, rapid progression with or without limb weakness, paresthesia, and decreased or absent DTR and albumin-cytological dissociation. Shahid Beheshti University of Medical Sciences 2014 /pmc/articles/PMC3943056/ /pubmed/24665332 Text en 2014: Iranian Journal of Child Neurology This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Letter to Editor
INALOO, Sorour
KATIBEH, Pegah
Guillain-Barre Syndrome Presenting With Bilateral Facial Nerve Palsy
title Guillain-Barre Syndrome Presenting With Bilateral Facial Nerve Palsy
title_full Guillain-Barre Syndrome Presenting With Bilateral Facial Nerve Palsy
title_fullStr Guillain-Barre Syndrome Presenting With Bilateral Facial Nerve Palsy
title_full_unstemmed Guillain-Barre Syndrome Presenting With Bilateral Facial Nerve Palsy
title_short Guillain-Barre Syndrome Presenting With Bilateral Facial Nerve Palsy
title_sort guillain-barre syndrome presenting with bilateral facial nerve palsy
topic Letter to Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3943056/
https://www.ncbi.nlm.nih.gov/pubmed/24665332
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