Rate the Article: Amsan Variant of Guillain-Barresyndrome: A Case Report, IJSR, Call for Papers, Online Journal
International Journal of Science and Research (IJSR)

International Journal of Science and Research (IJSR)
Call for Papers | Fully Refereed | Open Access | Double Blind Peer Reviewed

ISSN: 2319-7064

Downloads: 95 | Views: 285

Case Studies | Pharmacotherapeutics | India | Volume 8 Issue 8, August 2019 | Rating: 6.6 / 10


Amsan Variant of Guillain-Barresyndrome: A Case Report

Anzon John


Abstract: Guillain- Barré syndrome (GBS) is a rare and potentially life-threatening medical condition resulting from an individual’s immune system’s attack on the peripheral nerves. It is the result of an auto-immune response leading to axonal degeneration or demyelination. Acute motor and sensory axonal neuropathy (AMSAN) is a variant of GBS with the poorest prognosis. It is characterized by rapid-onset motor weakness, loss of deep tendon reflexes and sensory changes. Immunotherapy is considered a standard treatment for GBS. Here, the reported case is of AMSAN variant of GBS in a 42-year-old patient, who developed bilateral facial nerve palsy and treated with intravenous immunoglobulin (IVIg).


Keywords: immune system, deep-tendon reflexes, lower and upper limbs, muscle movement


Edition: Volume 8 Issue 8, August 2019,


Pages: 1955 - 1957



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