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Guillain–Barre syndrome with hyperreflexia: A variant

Guillain–Barre syndrome (GBS) is a common cause of acute peripheral neuropathy and is characterized by hyporeflexia or areflexia. Hyperreflexia has been rarely reported with acute motor axonal neuropathy. A 10-year-old boy presented with asymmetrical weakness of upper and lower limbs and change of v...

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Autores principales: Singhal, Vikram, Bhat, Kamalakshi G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3296413/
https://www.ncbi.nlm.nih.gov/pubmed/22408668
http://dx.doi.org/10.4103/1817-1745.92844
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author Singhal, Vikram
Bhat, Kamalakshi G.
author_facet Singhal, Vikram
Bhat, Kamalakshi G.
author_sort Singhal, Vikram
collection PubMed
description Guillain–Barre syndrome (GBS) is a common cause of acute peripheral neuropathy and is characterized by hyporeflexia or areflexia. Hyperreflexia has been rarely reported with acute motor axonal neuropathy. A 10-year-old boy presented with asymmetrical weakness of upper and lower limbs and change of voice. Weakness progressed in the hospital with involvement of multiple cranial nerves, preserved deep tendon jerks with extensor plantar, and normal abdominal reflexes. He was treated with IV immunoglobulin and IV methylprednisolone. He was able to walk with support with normal voice at the time of discharge. GBS should be a differential diagnosis in patients with acute quadriparesis even if there are preserved deep tendon reflexes.
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spelling pubmed-32964132012-03-09 Guillain–Barre syndrome with hyperreflexia: A variant Singhal, Vikram Bhat, Kamalakshi G. J Pediatr Neurosci Case Report Guillain–Barre syndrome (GBS) is a common cause of acute peripheral neuropathy and is characterized by hyporeflexia or areflexia. Hyperreflexia has been rarely reported with acute motor axonal neuropathy. A 10-year-old boy presented with asymmetrical weakness of upper and lower limbs and change of voice. Weakness progressed in the hospital with involvement of multiple cranial nerves, preserved deep tendon jerks with extensor plantar, and normal abdominal reflexes. He was treated with IV immunoglobulin and IV methylprednisolone. He was able to walk with support with normal voice at the time of discharge. GBS should be a differential diagnosis in patients with acute quadriparesis even if there are preserved deep tendon reflexes. Medknow Publications & Media Pvt Ltd 2011 /pmc/articles/PMC3296413/ /pubmed/22408668 http://dx.doi.org/10.4103/1817-1745.92844 Text en Copyright: © Journal of Pediatric Neurosciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Singhal, Vikram
Bhat, Kamalakshi G.
Guillain–Barre syndrome with hyperreflexia: A variant
title Guillain–Barre syndrome with hyperreflexia: A variant
title_full Guillain–Barre syndrome with hyperreflexia: A variant
title_fullStr Guillain–Barre syndrome with hyperreflexia: A variant
title_full_unstemmed Guillain–Barre syndrome with hyperreflexia: A variant
title_short Guillain–Barre syndrome with hyperreflexia: A variant
title_sort guillain–barre syndrome with hyperreflexia: a variant
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3296413/
https://www.ncbi.nlm.nih.gov/pubmed/22408668
http://dx.doi.org/10.4103/1817-1745.92844
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