Multiple Cranial Neuropathies Without Limb Involvements: Guillain-Barre Syndrome Variant?

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Multiple Cranial Neuropathies Without Limb Involvements: Guillain-Barre Syndrome Variant?

Acute multiple cranial neuropathies are considered as variant of Guillain-Barre syndrome, which are immune-mediated diseases triggered by various cases. It is a rare disease which is related to infectious, inflammatory or systemic diseases. According to previous case reports, those affected can exhibit almost bilateral facial nerve palsy, then followed by bulbar dysfunctions (cranial nerves IX ...

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Miller-Fisher variant of Guillain-Barre syndrome.

The authors declare that the material here submitted is original and is not currently under consideration nor has been accepted for publication elsewhere. All authors have read the manuscript and approved its submission. The authors have reported to the ACCP that no significant conflicts of interest exist with any companies/organizations whose products or services may be discussed in this artic...

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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 voice. Weakness progressed in the hospital with involvement of multiple cranial nerves, preserved ...

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Guillain-Barre’ Syndrome: A Case Report

Background and Objectives: Guillain-Barre´ Syndrome (GBS) is an acute-onset, monophasic, immune-mediated polyneuropathy that often follows an antecedent infection. Special nutritional support has an important role in these patients. Methods: A 6 years old girl with GBS was admitted to PICU of Dr. Sheikh Children Hospital (Mashhad, Iran). Chief compliance for hospitalization was inability to w...

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ژورنال

عنوان ژورنال: Annals of Rehabilitation Medicine

سال: 2013

ISSN: 2234-0645,2234-0653

DOI: 10.5535/arm.2013.37.5.740